ISO Certification Consultancy

We are a leading Service Provider of export to saudi arabia_certificate of conformity (coc), combined ul mark for europe canada and united states, iso 6346:1995 freight containers, iso 14024:2018 type i environmental labelling principles and procedures, iso 14009:2020 guidelines for incorporating material circulation in design and development and mutual recognition of certification from Palwal, India.

Export to Saudi Arabia_Certificate of Conformity (CoC)

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Type Of IndustryManufacturing
Mode Of ReportOffline
Type of CertificationRenewal
Type Of Service ProviderConsulting Firm
The Kingdom of Saudi Arabia requires that all consignments of products to be exported to the country should be accompanied by a Certificate of Conformity (COC). This testifies their compliance with the applicable standards and technical regulations.

The Kingdom of Saudi Arabia requires that all consignments of products to be exported to the country should be accompanied by a Certificate of Conformity (CoC). This testifies their compliance with the applicable standards and technical regulations.

We offer various services to help clients through the process of compliance of the conformity assessment program. Depending on the nature of the product, the verification may involve one or a combination of the following activities:

  • Physical inspection prior to shipment
  • Sampling, testing and analysis in accredited laboratories
  • Audit of product manufacturing processes
  • Documentary check and assessment of conformity with the requirements of the applicable technical regulations and standards, for example SASO, GSO, IEC

The Conformity Assessment program is under the authority of the Ministry of Commerce and Industry

Our extensive experience in managing conformity assessment programs around the globe enables us to offer efficient, comprehensive and tailored solutions to exporters and make sure their shipments are in conformity with applicable requirements.

Combined UL Mark for Europe Canada And United States

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Type Of IndustryManufacturing
Mode Of ReportHard Copy
Location/CityMumbai
Type of CertificationRenewal
Type Of Service ProviderConsulting Firm

Products in compliance with UL’s Listing and Follow-Up Service for Canada and the United States as well as our certification service for Europe and factory inspection requirements are eligible to bear a combined UL Mark for all three markets.

There are two options for the combined mark

The combined UL Mark for Europe, Canada and the United States generally includes the following:

  • UL in a circle symbol with C, US an EU identifiers
  • Word Listed
  • Alphanumeric control number
  • Product category name (product identifier) as indicated in UL’s certification directory

A manufacturer’s name or trademark, and model number are also required on the product.
When applicable, a combined UL Mark for Europe, Canada and the United States may only be applied while a product remains in compliance with all certification programs represented by the combined version of the mark. Products found to be noncompliant with the terms, conditions or other UL requirements of any of the certification programs for Europe, Canada or the United States are ineligible to bear a combined mark. However, these products can continue to bear individual UL Marks for specific certification programs as long as a product continues to comply with UL’s requirements.

The UL Enhanced and Smart Marks for the United States, Canada and Europe consist of:

  • The basic Enhanced Mark
  • SAFETY attribute
  • ISO country code of CA for Canada, EU for Europe and US for the United States
  • Unique identifier
  • Optional QR code for the smart version

Additionally, a product name and issue/serial number or alphanumeric control number may also appear on a certified product.

A manufacturer’s name or trademark, and model number are also required on the product.

ISO 6346:1995 Freight containers

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Container Lengthcertificate
Type of CertificationNew Certification
Type Of IndustryManufacturing
Mode Of ReportHard Copy
Location/CityPan India

Minimum order quantity: 2 Piece

ISO 6346 is an international standard covering the coding, identification and marking of intermodal (shipping) containers used within containerized intermodal freight transport.[1] The standard establishes a visual identification system for every container that includes a unique serial number (with check digit), the owner, a country code, a size, type and equipment category as well as any operational marks. The standard is managed by the International Container Bureau

ISO 14024:2018 Type I environmental labelling Principles and procedures

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ISO19990
ISO 14024:2018 establishes the principles and procedures for developing Type I environmental labelling programmes, including the selection of product categories, product environmental criteria and product function characteristics, and for assessing and demonstrating compliance. ISO 14024:2018 also establishes the certification procedures for awarding the label

ISO 14009:2020 Guidelines for incorporating material circulation in design and development

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ISO19990

This document gives guidelines for assisting organizations in establishing, documenting, implementing, maintaining and continually improving material circulation in their design and development in a systematic manner, using an environmental management system (EMS) framework.

These guidelines are intended to be used by those organizations that implement an EMS in accordance with ISO 14001. The guidelines can also help in integrating material circulation strategies in design and development when using other management systems. The guidelines can be applied to any organization regardless of its size or activity.

This document provides guidelines for design strategies on material circulation to achieve the material efficiency objectives of an organization, by focusing on the following aspects:

— type and quantity of materials in products;

— product lifetime extension;

— recovery of products, parts and materials.

In design and development, many aspects are considered, such as safety, energy efficiency, performance and cost. Although important, they are not addressed in this document.

Mutual Recognition Of Certification

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Type Of IndustryManufacturing
Mode Of ReportOffline
Location/CityMumbai
Type of CertificationRenewal
Type Of Service ProviderConsulting Firm

System UkrSEPRO has exclusive rights to the recognition of certification results in other countries to meet the requirements of normative documents of Ukraine. As a result, the certificate is issued or a certificate of conformity.

     Ukraine has concluded bilateral intergovernmental agreement on mutual recognition of certification results. These agreements were concluded with the countries - former republics of the Soviet Union, with which Ukraine has a common (harmonized) legal framework. They are: Russian Federation, Belarus, Uzbekistan, Armenia, Kyrgyz Republic, Georgia, Azerbaijan, Kazakhstan, Turkmenistan, Republic of Moldova Republic of Tajikistan. It should be emphasized that the recognition of conformity certificates issued by these countries, is made only for products manufactured in this country. That is, the system UkrSEPRO does not provide for recognition of conformity certificates issued by, for example, in Russia, the products produced, such as Europe.

It should be noted that certificates of compliance can be recognized, mostly for party products entering the customs territory of Ukraine, with the issued Certificate of Recognition.

     May recognize the certification tests, then examined the production or certification (assessment) quality management system can issue certificates of conformity for products for a period of 2 years or 5 years without taking a certification test.

     In all cases, recognition is possible and done in the case of coincidence of regulatory documents.

     The work on recognition of the results of product certification in the OS are available:

     • an application for works to recognize the results of product certification;

     • a set of documents in accordance with the list of documents submitted with the application for recognition of the results of product certification in the countries mentioned above.

Burundi_Pre-Shipment Verification of Conformity (PVoC)

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Type Of IndustryFood
Mode Of ReportHard Copy
Location/CityMumbai
Type of CertificationRenewal

The Burundi Bureau of Standards and Quality Control (BBN) has introduced its own Pre-Shipment Verification of Conformity (PVoC) Program, bringing the country into line with other State Members of the East African Community. This scheme has been designed to protect consumer health and safety by ensuring that goods imported to Burundi conform to applicable local, regional and/or international standards.  

Depending on the certification route, we provide one or a combination of the following interventions:

  • Physical inspection prior to shipment
  • Sampling, testing and analysis in accredited laboratories
  • Audit of product manufacturing processes
  • Documentary check and assessment of conformity with the requirements of the applicable standards
Why choose PCA ?

With extensive experience in managing conformity assessment programs , we have a global network of experts . We offer exporters efficient, comprehensive and tailored solutions to ensure shipments conform to Burundi’s program and its standards.

Export to Qutar_Certificate Of Conformity (coc)

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Type Of IndustryManufacturing
Mode Of ReportHard Copy
Location/CityMumbai
Type of CertificationRenewal
Type Of Service ProviderConsulting Firm
Pre-Shipment Conformity Verification for Qatar from our associate – enabling organizations to export and sell goods to the Qatari market.

Pre-Shipment Conformity Verification for Qatar from our associate – enabling organizations to export and sell goods to the Qatari market.

The Qatar Ministry of Environment’s (MOE) Qatar General Organization for Standards and Metrology (QGOSM) has implemented a pre-shipment verification of conformity scheme to protect the public against substandard products and prohibit entry to debased and fake products. The scheme requires all regulated imported products as defined by QGOSM, to be accompanied by certificate of conformity issued by an approved third party.

We are approved as a third party company to conduct an assessment against the standards and on successful completion issue a certificate of conformity (CoC) for the export of regulated products to Qatar. Application for assessment and a CoC should be made by the exporter in the country of supply. We will verify:

  • The description and specification of the goods
  • The conformity with the relevant Qatari standards and Qatari Technical Regulations or their approved Gulf or International standards

A Certificate of Conformity shall be issued once the evaluation results in a ‘SATISFACTORY’ result against the Qatari requirements.

The following products are the regulated in the Qatari conformity program:

  1. Brake Pads
  2. Safety Belts
  3. Wheel Rims
  4. Electric Irons
  5. Exhaust Fans
  6. Hair Dryers

With decades of experience managing conformity assessment programs, we offers exporters efficient and comprehensive solutions to ensure shipments conform to Qatar’s requirements.

Marks for UL Energy Verification Service

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Type Of IndustryIT and Consulting
Mode Of ReportOnline
Location/CityPan India
Type of CertificationNew Certification
Type Of Service ProviderConsulting Firm
The UL Energy Mark appears on air conditioners and furnaces, refrigerators and freezers, dishwashers, washers and dryers, water heaters, cooking equipment, and similar products evaluated to U.S. and Canadian energy efficiency standards. These products are already certified for safety by UL before earning the UL Energy Mark.

The UL Enhanced and Smart Marks for the United States and Canada for energy certification appear as above.

An optional QR code may also appear in these marks.

ISO 35001:2019 Biorisk management for laboratories and other related organisations

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Certifications ProvidedISO 35001:2019 Biorisk management for laboratories and other related organisations
Target LocationPan India
Document verification ModeOffline
Training Courses (if applicable)ISO 35001:2019 Biorisk management for laboratories and other related organisations
Services offeredConsultancy
Type of CertificationNew Certification
Type of IndustryFor IT and Consulting
Mode of ReportHard Copy
Service Duration1 to 3 Month
Response TimeSame time

Minimum order quantity: 1 Certificate

This document defines a process to identify, assess, control, and monitor the risks associated with hazardous biological materials. This document is applicable to any laboratory or other organization that works with, stores, transports, and/or disposes of hazardous biological materials. This document is intended to complement existing International Standards for laboratories.

This document is not intended for laboratories that test for the presence of microorganisms and/or toxins in food or feedstuffs. This document is not intended for the management of risks from the use of genetically modified crops in agriculture.

ISO/IEC CD 42001.2 Information Technology Artificial intelligence Management system

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Certifications ProvidedISO/IEC CD 42001.2 Information Technology - Artificial intelligence - Management system
Target LocationPan India
Document verification ModeOffline
Training Courses (if applicable)ISO/IEC CD 42001.2 Information Technology - Artificial intelligence - Management system
Services offeredConsultancy
Type of CertificationNew Certification
Type of IndustryFor IT and Consulting
Mode of ReportHard Copy
Service Duration1 to 3 Month
Response TimeSame time

Minimum order quantity: 1 Certificate

“As AI technologies fuel the digital transformation, there has never been a more relevant time for international standards development. Our programme continues to grow and dynamically react to emerging industry needs, leveraging an ecosystem approach to accelerate AI adoption whilst simultaneously addressing concerns such as trustworthiness, ethics and societal concerns”, said Wael William Diab, Chair of SC 42.

Iso 13485 2016 Certification

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Type of CertificationNew Certification
Type Of IndustryManufacturing
Type Of Service ProviderConsulting Firm
Ensuring confidence in medical device safety

The medical device industry is affected by a complex array of regulatory systems, national and international standards and other requirements.


Whatever devices organization''''s produce, as medical device manufacturer/s, they have the  responsibility to consistently deliver devices that are safe and effective. ISO 13485 is the international standard recognized for medical device regulations around the world.


In the field of medical products, devices and components, regulatory requirements and customer needs regarding quality are becoming ever-more stringent. Legal manufacturers and their global suppliers are expected to pro-actively comply with the highest standards and regulations. Certification is needed before entering new markets or before customers place orders. ISO 13485 is now the foundation for all regulatory requirements.


Gaining certification to ISO 13485 will help organization do business in this highly regulated sector. Whether organization''''s are looking to operate internationally or to expand locally to accommodate new business, ISO 13485 will help demonstrate to customers and regulators that they are committed to quality.


The regular assessment process will ensure that processes are continually checked for effectiveness and provide the opportunity to avoid unpleasant regulatory surprises. Certification to this standard can improve overall performance, remove uncertainty and widen market opportunities with complying to requirements, such as:

  • Basic Quality System requirements with several enhancements
  • Risk Management Approach to product development and product realization
  • Validation of processes
  • Consideration of statutory and regulatory requirements
  • Tracking and record keeping
  • Assuring positive product traceability and recall

Who it is relevant to :
ISO 13485 is relevant to all manufacturers of medical devices (including subcontract manufacturers) to satisfy both regulatory and voluntary requirements.


Benefits :

  • ISO 13485 or in combination with regulatory certification, will be viewed by organization''''s customers, distributors and authorities as a genuine commitment to the quality of medical devices during the approval or bidding process.
  • Most medical device manufacturers will eventually want to sell their products worldwide. Certification to this standard will help achieve this objective.
  • Regular assessments performed by Zenith will help organization''''s to monitor and improve their management system and processes. This improves the reliability of operations and products, ensures compliance with regulatory and customer requirements and increases financial performance.

ISO 33001: 2015 Information technology Process Assessment

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ISO 33001 201520000

Minimum order quantity: 1 Certificate

About ISO/IEC 33001

Full title: ISO/IEC 33001:2015 — Information Technology — Process Assessment — Concepts and Terminology

So, ISO/IEC 33001 does exist — but note that it is part of the ISO/IEC (Information Technology) standards, not industrial management like ISO 9001.

📖 Overview of ISO/IEC 33001:2015 🔧 Purpose

ISO/IEC 33001:2015 provides the foundational concepts and terminology used in process assessment frameworks for information technology and software development.

It sets the basis for:

  • Assessing process capability

  • Improving process performance

  • Comparing organizational maturity

🧭 Key Points
AspectDescription
Standard Name ISO/IEC 33001:2015
Title Information Technology — Process Assessment — Concepts and Terminology
Replaces ISO/IEC 15504-1:2004 (SPICE Part 1)
Focus Defines concepts and terms for process assessment and capability determination
Used For Assessing and improving IT, software, and business processes
Applicable To Software organizations, IT service providers, process improvement teams
Supports Other ISO/IEC 33000-series standards (e.g., 33002, 33003, 33020)
📚 Other Related ISO/IEC 33000 Standards
StandardTitlePurpose
ISO/IEC 33002:2015 Requirements for performing process assessment Defines how to conduct assessments
ISO/IEC 33003:2015 Requirements for process measurement frameworks Establishes rules for measurement models
ISO/IEC 33004:2015 Requirements for process reference and assessment models Describes how models should be structured
ISO/IEC 33020:2019 Process measurement framework for assessment of process capability Used to measure maturity or capability levels
🧩 Where It’s Used
  • Software development and IT service companies

  • Organizations implementing CMMI-like maturity models

  • Enterprises seeking to benchmark or improve process capability

  • Consultants performing process capability assessments under ISO/IEC 330xx standards

A company developing software might use ISO/IEC 33001 as the conceptual base and ISO/IEC 33020 to measure their process maturity from Level 1 (Performed) to Level 5 (Optimizing).

ISO/IEC 23894 Information technology Artificial intelligenc Guidance on risk management

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ISOIEC2389420000

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Full title: ISO/IEC 23894:2023 — Information technology — Artificial intelligence — Guidance on risk management. Published: February 6, 2023. Scope: Provides guidance for organizations that develop, produce, deploy or use AI systems (products, services) on how to manage risks specific to AI. It helps integrate risk management into AI-related activities, and describes processes for implementing and integrating AI risk management.
 Structure / Key Clauses

The standard is divided roughly into three main parts (clauses) after initial definitions:

ClauseContent / Focus
Clause 4 — Principles Foundational guiding principles for AI risk management. These are high-level values or rules that should underpin all AI risk work.

Clause 5 — Framework
Guidance on setting up a risk management framework specific to AI: aligning leadership, policy, roles & responsibilities, integrating RM into governance, establishing communication & consultation, resources, continual improvement, etc.

Clause 6 — Processes
The operational part: how to perform risk management in practice — identifying risks, analyzing & evaluating them, treating them, monitoring & reviewing, recording & reporting. Customized for AI-specific challenges.

What differentiates ISO/IEC 23894 (vs more general risk management standards like ISO 31000) are some added or emphasized points specific to AI:
  • Use of normative references like ISO 31000:2018 (Risk Management Guidelines), ISO/IEC 22989:2022 (AI concepts & terminology), and ISO Guide 73 for risk vocabulary. 

  • Emphasis on risks that are more unique to AI, such as bias, fairness, transparency/explainability, robustness/adversarial vulnerabilities, data issues (data quality, data poisoning), ethics, legal & regulatory compliance for AI use‐cases.

How It Relates With Other Standards / What It Builds On
  • It is supplemental to ISO 31000:2018 (general risk management) — meaning ISO 23894 uses the framework of ISO 31000 but gives extra AI-specific guidance.

  • Here are some of the practical/pragmatic recommendations or takeaways (inferred from the guidance) that organizations should keep in mind:

    • Define the organizational context: what AI systems are being used, for what purpose, what are the stakeholders, environment, regulatory constraints etc.

    • Establish leadership commitment: senior management buy-in, clear policy concerning AI risk, allocating resources etc.

    • Identify potential risk categories early: including technical, ethical, legal, social, safety, privacy, security risks.

    • Perform risk assessments: combining likelihood & impact, considering uncertainties.

    • Treat / mitigate risks: via technical controls (e.g. model robustness, testing, validation), governance (oversight boards), processes (data checks, audits) etc.

    • Record & report risk decisions, maintain traceability and documentation.

    • Monitor AI system in deployment: track performance drift, emerging behaviors, external changes, regulatory changes.

     

 
 

ISO/IEC 19941:2017 Information technology Cloud computing Interoperability and portability

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ISO20000

ISO/IEC 19941:2017 specifies cloud computing interoperability and portability types, the relationship and interactions between these two cross-cutting aspects of cloud computing and common terminology and concepts used to discuss interoperability and portability, particularly relating to cloud services.

ISO/IEC 19941:2017 is related to other standards, namely, ISO/IEC 17788, ISO/IEC 17789, ISO/IEC 19086‑1, ISO/IEC 19944, and in particular, references the cross-cutting aspects and components identified in ISO/IEC 17788 and ISO/IEC 17789 respectively

ISO/IEC 38503:2022 Information technology Governance of IT Assessment of the governance of IT

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ISO20000

This document provides guidance on the assessment of governance of information technology (IT) based on the principles, definitions and model for the governance of IT outlined in ISO/IEC 38500 and ISO/IEC TR 38502 and the implementation considerations outlined in ISO/IEC TS 38501.

This document includes approaches for conducting the assessment, the criteria against which the assessment can be made, guidance on the evidence that can be used for the assessment, as well as a method for determining the maturity of the organization’s governance of IT.

This document is applicable to organizations of all sizes, regardless of the extent of their use of IT.

Reach Certification Service

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Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) is a European Union regulation dating from 18 December 2006. REACH addresses the production and use of chemical substances, and their potential impacts on both human health and the environment. Its 849 pages took seven years to pass, and it has been described as the most complex legislation in the Union's history and the most important in 20 years.It is the strictest law to date regulating chemical substances and will affect industries throughout the world. REACH entered into force on 1 June 2007, with a phased implementation over the next decade. The regulation also established the European Chemicals Agency, which manages the technical, scientific and administrative aspects of REACH.

Overview

When REACH is fully in force, it will require all companies manufacturing or importing chemical substances into the European Union in quantities of one tonne or more per year to register these substances with a new European Chemicals Agency (ECHA) in Telakkakatu (Helsinki)  Finland. Since REACH applies to some substances that are contained in objects (articles in REACH terminology), any company importing goods into Europe could be affected.

The European Chemicals Agency has set three major deadlines for registration of chemicals. In general these are determined by tonnage manufactured or imported, with 1000 tonnes/a. being required to be registered by 1 December 2010, 100 tonnes/a. by 1 June 2013 and 1 tonne/a. by 1 June 2018.In addition, chemicals of higher concern or toxicity also have to meet the 2010 deadline.

About 143,000 chemical substances marketed in the European Union were pre-registered by the 1 December 2008 deadline. Although pre-registering was not mandatory, it allows potential registrants much more time before they have to fully register. Supply of substances to the European market which have not been pre-registered or registered is illegal (known in REACH as "no data, no market").

 

The European Commission supports businesses affected by REACH by handing out – free of charge – a software application (IUCLID) that simplifies capturing, managing, and submitting data on chemical properties and effects. Such submission is a mandatory part of the registration process. Under certain circumstances the performance of a chemical safety assessment (CSA) is mandatory and a chemical safety report (CSR) assuring the safe use of the substance has to be submitted with the dossier. Dossier submission is done using the web-based software REACH-IT.

The aim of REACH is to improve the protection of human health and the environment by identification of the intrinsic properties of chemical substances. At the same time, innovative capability and competitiveness of the EU chemicals industry should be enhanced.

ISO 14025:2006 Environmental labels and declaration

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ISO20000
ISO 14025:2006 Environmental labels and declarations — Type III environmental declarations — Principles and procedures

ISO 14025:2006 establishes the principles and specifies the procedures for developing Type III environmental declaration programmes and Type III environmental declarations. It specifically establishes the use of the ISO 14040 series of standards in the development of Type III environmental declaration programmes and Type III environmental declarations.

ISO 17987-2:2025 Transport protocal and Network Layer Service.

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ISO19990

This document specifies a transport protocol and network layer services tailored to meet the requirements of LIN‑based vehicle network systems on local interconnect networks. The protocol specifies an unconfirmed communication.

The LIN protocol supports the standardized service primitive interface as specified in ISO 14229-2.

This document provides the transport protocol and network layer services to support different application layer implementations such as:

—     normal communication messages, and

—     diagnostic communication messages.

The transport layer defines transportation of data that is contained in one or more frames. The transport layer messages are transported by diagnostic frames. A standardized API is specified for the transport layer.

ISO/IEC 20000-1:2018 - Information technology

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ISO20000

This document specifies requirements for an organization to establish, implement, maintain and continually improve a service management system (SMS). The requirements specified in this document include the planning, design, transition, delivery and improvement of services to meet the service requirements and deliver value. This document can be used by:

a) a customer seeking services and requiring assurance regarding the quality of those services;

b) a customer requiring a consistent approach to the service lifecycle by all its service providers, including those in a supply chain;

c) an organization to demonstrate its capability for the planning, design, transition, delivery and improvement of services;

d) an organization to monitor, measure and review its SMS and the services;

e) an organization to improve the planning, design, transition, delivery and improvement of services through effective implementation and operation of an SMS;

f) an organization or other party performing conformity assessments against the requirements specified in this document;

g) a provider of training or advice in service management.

ISO/IEC 22603-1:2021 Information Technology

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ISo20000
This document establishes the general requirements for electronic product labelling which can be applicable to all types of product regardless of industry.

ISO 59004 Circular Economy Terminology, Principles and Guidance for Implementation

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ISO20000

This document defines key terminology, establishes circular economy principles, and provides guidance for its implementation by using a framework and areas of action.

It is intended to be used by organizations seeking to understand and commit to a circular economy while contributing to sustainable development. These organizations can be either private or public, acting individually or collectively, regardless of type or size, and located in any jurisdiction, or position within a specific value chain or value network.

Iso 14045:2012 Eco-Efficiency Assessment Of Product Systems Principles, Requirements And Guidelines

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ISO19990

ISO 14045:2012 describes the principles, requirements and guidelines for eco-efficiency assessment for product systems including:

  1. the goal and scope definition of the eco-efficiency assessment;
  2. the environmental assessment;
  3. the product-system-value assessment;
  4. the quantification of eco-efficiency;
  5. interpretation (including quality assurance);
  6. reporting;
  7. critical review of the eco-efficiency assessment.

Requirements, recommendations and guidelines for specific choices of categories of environmental impact and values are not included. The intended application of the eco-efficiency assessment is considered during the goal and scope definition phase, but the actual use of the results is outside the scope of ISO 14045:2012.


Iso 14026:2017 Principles, Requirements And Guidelines For Communication Of Footprint Information

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ISO19990

ISO 14026:2017 provides principles, requirements and guidelines for footprint communications for products addressing areas of concern relating to the environment.

ISO 14026:2017 also provides requirements and guidelines for footprint communication programmes, as well as requirements for verification procedures.

ISO 14026:2017 does not address the quantification of a footprint, nor does it address the communication of footprints that are not related to the environment, e.g. footprints addressing social or economic issues. In particular, footprint communications relating to the economic and social dimensions of sustainable development are outside the scope of ISO 14026:2017. Footprint communications relating to organizations are also outside the scope of ISO 14026:2017.

ISO 14051:2011 Environmental management Material flow cost accounting General framework

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ISO 1405119990
ISO 14051:2011 provides a general framework for material flow cost accounting (MFCA). Under MFCA, the flows and stocks of materials within an organization are traced and quantified in physical units (e.g. mass, volume) and the costs associated with those material flows are also evaluated. The resulting information can act as a motivator for organizations and managers to seek opportunities to simultaneously generate financial benefits and reduce adverse environmental impacts. MFCA is applicable to any organization that uses materials and energy, regardless of their products, services, size, structure, location, and existing management and accounting systems.

ISO 14007:2019 Guidelines for determining environmental costs and benefits

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This document gives guidelines for organizations on determining the environmental costs and benefits associated with their environmental aspects. It addresses the dependencies of an organization on the environment, for example, natural resources, and the context in which the organization operates or is located. Environmental costs and benefits can be expressed quantitatively, in both non-monetary and monetary terms, or qualitatively.

This document also provides guidance for organizations when disclosing related information.

This document takes an anthropocentric perspective, i.e. looking at changes that affect human wellbeing (utility) including their concern for, and dependence on, nature and ecosystem services. This includes use and non-use values as reflected in the concept of total economic value when environmental costs and benefits are determined in monetary terms.

The ways in which the environmental costs and benefits are used after they have been determined are outside the scope of this document.

This document is applicable to any organization regardless of size, type and nature.

ISO/IEC 17825:2024 Information Technology

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StandardISO/IEC 17825:2024
LocationPan India
Document VerificationOnline

Minimum order quantity: 1 Certificate

This document specifies the non-invasive attack mitigation test metrics for determining conformance to the requirements specified in ISO/IEC 19790:2012 for security levels 3 and 4. The test metrics are associated with the security functions addressed in ISO/IEC 19790:2012. Testing is conducted at the defined boundary of the cryptographic module and the inputs/outputs available at its defined boundary.

This document is intended to be used in conjunction with ISO/IEC 24759:2017 to demonstrate conformance to ISO/IEC 19790:2012.

ISO/TS 32001-2:2022 - Document management

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StandardISO/TS 32001
LocationPan India
Document VerificationOnline

This document specifies how to extend the specifications in ISO 32000-2 by adding support for the use of the Secure Hash Algorithm – 3 (SHA-3) and SHAKE256 hash algorithms.

This document does not specify the following:

—    specific processes for converting paper or electronic documents to the PDF file format;

—    specific technical design, user interface implementation, or operational details of rendering;

—    specific physical methods of storing these documents such as media and storage conditions;

—    methods for validating the conformance of PDF files or PDF processors;

—    required computer hardware and/or operating system

Marks for UL Classification Service

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Type Of IndustryIT and Consulting
Mode Of ReportOffline
Location/CityDelhi
Type of CertificationRenewal

UL’s Marks for our Classification service appear on representative samples of products that UL has evaluated with respect to specific properties, a limited range of hazards or suitability for use under limited or special conditions.

There are also multiple variations of marks for UL’s Classification service, some of which are used in the United States, others used in Canada and still others used in both markets. Products carrying marks for Canada have been evaluated to Canadian standards for a specific hazard or property. A combination mark indicates compliance with both Canadian and U.S. requirements.

In the Classification service, UL determines that a manufacturer has demonstrated the ability to produce a product complying with UL’s requirements with respect to one or more of the following:

  • Specific risk, e.g., casualty, fire, etc.
  • Performance under specific conditions
  • Compliance with regulatory codes
  • Compliance with specific standards such as international standards
  • Other condition, as determined by UL

All of the products carrying these marks are covered by UL’s Follow-Up Services program to determine that they continue to be manufactured in compliance with UL’s requirements.

There are two options for the marks for UL’s Classification service.

The UL Classification Marking appearing on a product typically consists of four required elements:

  • UL in a circle symbol
  • Word Classified
  • Product name or company name/file number
  • Issue/serial number or alphanumeric control number

 

Information identifying the scope of UL’s certification will also appear on the product.

The UL Enhanced and Smart Marks for the United States and Canada for the Classification service consist of:

  • The basic Enhanced Mark
  • SAFETY attribute
  • ISO country code of CA for Canada or US for the United States, or both CA and US
  • Unique identifier
  • Optional QR code for the smart version

Information identifying the scope of UL’s certification will also appear on the product.

 

Additionally, a product name and issue/serial number or alphanumeric 

Export To Usa And Canada_CSA Mark for Gas Filled Product

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Type Of IndustryFood
Mode Of ReportHard Copy
Location/CityDelhi
Type of CertificationRenewal
Type Of Service ProviderConsulting Firm
Indicates that the product was tested and has met the certification requirements for gas-fired products for USA

Certification Service

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Type Of IndustryManufacturing
Mode Of ReportOffline
Location/CityMumbai
Type of CertificationRenewal
Type Of Service ProviderConsulting Firm
ASME NQA-1 stands for American Society of Mechanical Engineer � Nuclear Quality Assurance. This certificate is awarded to those organization who is having capability for designs/manufacturing/supply of nuclear product or related products. If you are into the business of Electric power generation by Nuclear energy or manufacturer of X-Ray machine or Electro magnetic product/ Electrical product you can apply for this certification to prove your technical proficiency and capability. 8 ISO 13485.asp: ISO 13485 is for quality management system for medical devices this certificate is applicable for manufacturer, supplier and traders of medical devices. If you are designing, manufacturing, supplying, trading of various medical devices like syringe, medical testing equipment, bone cutter machine, medical equipments etc, you are eligible to get this certificate.

Quality Certification

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Location/CityPan India
Type of CertificationRenewal
Type Of IndustryManufacturing
Type Of Service ProviderConsulting Firm

Established in the year 2000, at Mumbai, Maharashtra, India, we “Deming Certification Services Pvt. Ltd.,” offer clients total certifications solutions that helps in enhancing systems and processes at their end. Further, the expertise of certifications personnel also assist us in changing the working pattern of several organizations by bringing positive change in their work culture as well as inculcating quality in every sphere of involved operations.

 

The solutions offered by us cover areas like ISO 9001 Certification, ISO 27001 Certification, ISO 14001 Certification, SQC/SPC  Certification, ISO 17025  Certification and ISO 22000 Certification. Apart from this, we also offer solutions for HACCP Certification, ISO/TS 16949 Certification, OHSAS 18001, Social Accountability Certification, Risk Assessment Services, ISO 20000 Certification, Project Management Certification, SA 8001 Certification and Third Party Inspection and Verification Services.

 

Our business operations are led by Mr. Mukesh Singh, who has with him rich experience in our industry sector. His visionary approach has also assisted us in emerging amongst fastest growing business management certification companies in our industry sector. Further, the service support provided by experienced industry professionals also allow us to offer clients a wide range of business certifications services for availing different certifications.

 

Today, our team of experts work in close coordination with clients and help them to access their specific requirements as well as add value to their systems. This is achieved through designing formats as well as assisting in implementation by continuous training, review of quality manual as well as undertaking other allied procedures. Other than this, the competitive prices of our services also makes them one of the most demanded in the market.

ISO 14044:2006

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ISO19990

ISO 14044:2006 specifies requirements and provides guidelines for life cycle assessment (LCA) including: definition of the goal and scope of the LCA, the life cycle inventory analysis (LCI) phase, the life cycle impact assessment (LCIA) phase, the life cycle interpretation phase, reporting and critical review of the LCA, limitations of the LCA, relationship between the LCA phases, and conditions for use of value choices and optional elements.

ISO 14044:2006 covers life cycle assessment (LCA) studies and life cycle inventory (LCI) studies.


Iso/Dtr 23585

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ISO26000

ISO/IEC 19941:2017 specifies cloud computing interoperability and portability types, the relationship and interactions between these two cross-cutting aspects of cloud computing and common terminology and concepts used to discuss interoperability and portability, particularly relating to cloud services.

ISO/IEC 19941:2017 is related to other standards, namely, ISO/IEC 17788, ISO/IEC 17789, ISO/IEC 19086‑1, ISO/IEC 19944, and in particular, references the cross-cutting aspects and components identified in ISO/IEC 17788 and ISO/IEC 17789 respectively.

ISO/IEC 30169:2022

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ISO20000
This document specifies the system framework, IoT application model and overall technical requirements for ELS. This document applies to the design and development of the IoT applications for ELS. The IoT applications for ELS specified in this document are mainly applicable to the retail industry, and can also provide reference for the design and development of the IoT applications for ELS in other industries.

LA 9001 Training

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What you will gain:
Higher Effectiveness and Efficiency on their JobExcellent
Career Enhancement Opportunity
Internationally Recognized Qualification
Photo-identity Card from ASCB(Europe) Ltd. - UKListing among an International list of Quality Professionals.


Established in the year 2000, at Mumbai, Maharashtra, India, we “Deming Certification Services Pvt. Ltd.,” offer clients total certifications solutions that helps in enhancing systems and processes at their end. Further, the expertise of certifications personnel also assist us in changing the working pattern of several organizations by bringing positive change in their work culture as well as inculcating quality in every sphere of involved operations.

 

The solutions offered by us cover areas like ISO 9001 Certification, ISO 27001 Certification, ISO 14001Certification, SQC/SPC Certification, ISO 17025 Certification and ISO 22000 Certification. Apart from this, we also offer solutions for HACCP Certification, ISO/TS 16949 Certification, OHSAS 18001, Social Accountability Certification, Risk Assessment Services, ISO 20000 Certification, Project ManagementCertification, SA 8001 Certification and Third Party Inspection and Verification Services.

 

Our business operations are led by Mr. Mukesh Singh, who has with him rich experience in our industry sector. His visionary approach has also assisted us in emerging amongst fastest growing business management certification companies in our industry sector. Further, the service support provided by experienced industry professionals also allow us to offer clients a wide range of business certifications services for availing different certifications.

 

Today, our team of experts work in close coordination with clients and help them to access their specific requirements as well as add value to their systems. This is achieved through designing formats as well as assisting in implementation by continuous training, review of quality manual as well as undertaking other allied procedures. Other than this, the competitive prices of our services also makes them one of the most demanded in the market.

UL Functional Safety Recognized Component Mark

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Mode Of ReportOffline
Location/CityMumbai
Type of CertificationRenewal
Type Of Service ProviderConsulting Firm

The Recognized Component Functional Safety Marks are specifically used on components that are part of larger products or systems intended to partially fulfill the functional safety requirements of the system. The Functional Safety Component Recognition will streamline the functional safety investigation of the final product/system since the component will have already been partially prequalified for the intended use.

For Functional Safety Recognized Components, manufacturers will provide instructions that include component ratings, application restrictions and intended safety level, such as Safety Integrity Level (SIL), Automotive Safety Integrity Level (ASIL), Performance Level (PL) or Class.

These components may have restrictions on their performance or may be incomplete in construction. Guidelines addressing the suitability of a component when used in an end product are noted in UL’s test report as conditions of acceptability.The suitability of the use of a functional safety component in a certain situation or for a particular safety level (SIL, ASIL, PL or Class) must be further evaluated within the context of the end-use application.

Just as with the UL Recognized Component Mark, there are three variations of UL’s Functional Safety Recognized Component Mark: one for the United States, one for Canada only and one for both the United States and Canada.

All components carrying the UL Functional Safety Recognized Component Mark are covered by UL’s Follow-Up Services program to determine continued compliance with UL’s requirements.

UL Energy Component Recognition Mark

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Type Of IndustryIT and Consulting
Mode Of ReportOnline
Location/CityPan India
Type of CertificationNew Certification
Type Of Service ProviderIndividual Consultant
Similar to UL’s Energy Mark for end products, the UL Energy Component Recognition Mark appears on components that meet UL’s requirements for safety as well as appropriate U.S. and Canadian energy efficiency standards. These components are used by manufacturers in end products sold in the U.S. and Canada marketplace.

Marks for UL Environmental And Public Health Certification

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Type Of IndustryManufacturing
Mode Of ReportOffline
Location/CityMumbai
Type of CertificationRenewal
Type Of Service ProviderConsulting Firm

The UL EPH Marks appears as above.

The EPH Listed Mark is typically used for products complying with UL’s own published Standards for Safety. The EPH Classified Mark is used for products complying with ANSI/NSF standards and other food equipment hygiene codes and requirements.

The UL Enhanced and Smart Marks for environmental and public health certification of food equipment appear .

 

An optional QR code may also appear in these marks.

UL Certified Water Quality Mark

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Type Of IndustryManufacturing
Mode Of ReportOffline
Location/CityMumbai
Type of CertificationRenewal
Type Of Service ProviderConsulting Firm
The UL Certified Water Quality Mark indicates that a manufacturer’s bottled water has demonstrated compliance with the requirements of UL’s Bottled Water Program. This rigorous program includes both United States regulations and supplemental industry standards. Bottled water bearing the mark has been verified for water quality.
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