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Certification Services #2861022

Integrated Management System Certification

The company is dedicatedly involved in offering a reliable Integrated Management System Certification service to the clients. Any organization can apply for an Integrated Management System irrespective of their size. This system helps the organization internally by reducing duplication and providing a centralized document control system. It also results in cost benefits in third party audits. The certifications such as ISO 9001, ISO 14001 and OHSAS 18001 have common elements between them. These can be easily integrated to a single, management system or in combination. We provide the facility of audit of joint systems. We help our clients in acquiring the Integrated Management System Certification with ease.

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ISO 13485 2013 Certification

The ISO 13485: 2013 Certification is a quality system certificate for organizations that design, develop, manufacture or service medical devices. If your company acquires an ISO 13485: 2013 Certification, it constructs a framework several regulatory and customer bodies like FDA. For obtaining it, our professionals make sure that organizations place special emphasis on meeting customer requirement and managing any hazards for specific designing and manufacturing of medical devices. Our ISO 13485: 2013 Certification services are reputed for their excellent value for money.

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ISO 20000-2011 ITSM Certification

Progressive ISO Certification India Private Limited is a name you can rely upon for all your need of ISO 20000:2011 ITSM Certification. We specialize in getting this certification to our clients. ISO 20000:2011 ITSM is an internationally recognized quality management system. We have talented people in our team that takes care of all the legalities involved in the acquisition of this certification. Our professionals suggest the clients with the best advice. They make sure that the client gets certified in the best manner possible. We operate from our headquarters in Bhopal (Madhya Pradesh)

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ISO 50001-2011 Energy Management System Certification

The ISO 50001:2011 is a certification that is essential for organizations that have implemented energy management systems. It certifies that the energy has been used more efficiently and is in compliance with the laid norms. Poor energy management can lead to wastage and environmental issues so this certification ensures better environmental contribution and a better economy. The clients can get in touch with Progressive ISO Certification India Private Limited, a Bhopal (Madhya Pradesh) service provider, now and avail its ISO 50001:2011 Energy Management System Certification service.

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ISO 14001-2015 EMS Certification

Get ISO 14001 : 2015 EMS Certification with our help. Our company is one of the eminent names in the industry offering reliable certification approval services. The ISO 14001 : 2015 EMS Certification is kept in high regard as it testifies for an organization’s credibility. Other reasons to get an ISO 14001 : 2015 EMS Certification are many customers only to do business with ISO Certified companies, it provides competitive advantage, real issues highlighted when external views of trained auditors is provided and organizations are motivated to keep on improving their quality standards when ISO Certification audits are impending.

This standard is applicable to any organization that wishes to :

  • Implement, maintain and improve an environmental management system.
  • Assure itself of its conformance with its own stated environmental policy (those policy commitments of course must be made).
  • Demonstrate conformance Ensure compliance with environmental laws and regulations Seek certification of its environmental management system by an external third party organization.
  • Make self-determination of conformance ISO14000 Environmental Management System The ISO 14001 standards are frameworks to provide an internationally recognized supporting for environmental management.
  • A system compliant to ISO 14001 is a management system dedicated to manage the environmental issues of an organization.
  • A Certified Environmental Management System means the business is taking active steps to fulfil social & environmental responsibilities.
  • Environmentally trustworthy companies have a competitive edge in national and international markets.
  • An "Environmental Management System" helps the organization to be in control and successfully manage the most significant environmental aspects, e.g. emissions, waste handling, utilize natural resources, rain water harvesting and energy-efficiency together with compliance to environmental regulations.


Some of the benefits of the ISO 14001 certification are :

  • Improved image of your organization in corporate level.
  • Mass Sacrifices Celebration of management responsibilities & commitment to environmental concerns towards employees, client & society.
  • Competitive advantage over international trade barriers.
  • Conforming to a rule with concerned statutory & regulatory requirements.
  • Help in converting by products and other waste into valuable forms.
  • Reduced energy consumption, hazards and accidents.
  • Effectively manage the significant environmental aspects.


ISO 14001 : 2015 is an environmental management standard. It defines a set of environmental management requirements for environmental management systems. The purpose of this standard is to help all kinds of organizations to protect the environment, to prevent pollution, and to improve their overall environmental performance.

This new ISO 14001 standard was officially published on November 15, 2015. It cancels and replaces the old ISO 14001 : 1996 standard. ISO 14001 : 1996 will expire on May 15, 2006. Therefore, you have until May 15, 2006 to make the transition to the new ISO 14001:2015 standard.

Since it was first published in 1996, ISO 14001 has rapidly become the most important environmental standard in the world. Thousands of organizations use it, environmentalists support it, and governments actively encourage its use. ISO 14001 applies to all types of organizations. It does not matter what size they are or what they do.

If you do not already have an environmental management system (EMS), you can use this ISO 14001 standard to establish one. In addition, once you have established your EMS, you can use it to manage the environmental aspects of your organization's activities, products and services, and to improve its overall environmental performance.

Environmental performance is all about how well you manage and control your environmental aspects and the impact they have on the environment.

You can also use this standard to demonstrate that you are doing everything you can to protect the environment and improve your environmental performance

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ISO OHSAS 18001-2007 Certification

Our company is engaged in providing ISO OHSAS 18001:2007 Certification to our clients all over India. Acquiring an ISO OHSAS 18001:2007 Certification for your organization means that you are targeting the health and safety of employees and proves that you are actively involved in ensuring that the work operations are safe for your employees as well as the surrounding environment. We have an efficient team of auditors and professionals that are proficient in all aspects of ISO OHSAS 18001:2007 Certification and will provide excellent guidance at any matter related to it. We are known for completing the job related to certification within the promised time.

 

ISO OHSAS 18001: 2007 Occupational Health and safety management Systems Specifications :

  • This standard prescribes requirements for an OH&SMS to enable an organization to formulate its policies and objectives to protect its employees and others, whose health and safety may be affected by the activities of the organization.
  • The extent of application depends on nature of activities, complexity of its operations.

 

Road Map for Occupational Health & Safety (ISO OHSAS) :

  • ISO OHSAS Policy to be displayed near the main gate

  • Register for reportable (More than 48Hrs rest) and non reportable (less than 48 Hrs rest) accidents or injury & Health Register as per Factory act 1948

  • Record of visit of Labor inspector /Factory inspector

  • Safety plan for all to combat natural calamity like flood, fire, drinking water to be analyzed to meet WHO requirement

  • Roads and walk way repair to prevent slip and fall and cause injury

  • Normal health check up record for all especially for diseases associated with occupational health

  • All noisy areas must have lot of open ventilation or high ceiling as per consent or people working must wear muff to avoid partial deafness

  • All bushes to be cut before summer which may cause fire

  • All water hydrants and fire extinguishers to be tested and record kept

  • All septic tanks to be cleaned once in a year

  • All canteen waste to be disposed in a proper way (Given to animals e.g. pigs)

  • Trees to be planted to prevent dust going into eyes and causing problem14. Record the visit of Health department official and vaccination dates

  • Record of mock drill for fire extinguishing

  • Training records of people including main supplier

  • Internal audit & management reviews

  • Complaint register to be available at gate

  • Fire prevention and emergency preparedness drill in case of natural calamity or disaster management

  • Health check up statement for every year

  • Safety record and use of safety appliance

  • All LPG cylinders to be tested for leakage and user to be trained

  • All licenses like factory, ESI registration for workmen, lift license

  • Pressure vessel license, oil storage license

  • Display at the gate following Workmen minimum wages act, Factory act 1948, Minor below 18 years not allowed d in factory premises

  • First aid box and ambulance on call

  • Health and safety budget

 

Following are the acts and regulatory requirements of the ISO OHSAS 18001:2007 Certification Applicable in INDIA :

  • Coverage of key issues-inclusive of The Water Act, 1974

  • The Water Cess Act, 1977

  • The Air Act, 1981

  • The Environment (Protection) Act, 1986

  • The Manufacture, Storage and Import of Hazardous

  • Chemical Rules, 1989/ 1994/ Amendment Rules, 2000

  • The Hazardous Waste (Management & Handling) Rules, 1989 and Amendment Rules, 2000

  • Gas Cylinder Rules, 1981, SMPV Rules, 1981

  • Indian Petroleum Rules, 1976

  • Factory Act, 1948

  • Noise Pollution and Control Rules, 2000

  • The Biomedical Waste Rules, 1998

  • The Explosive Act /Rules

  • Central Motor Vehicles Rules and others

 

Advantages Of ISO OHSAS 18001:2007 Certification :

  • Reduction of loss caused by professional accidents and illness

  • Greater work legal requirements compliance control

  • Customer and employee satisfaction

  • Greater trust from stockholders and investors

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ISO 22000-2018 Certification

We offer the best solutions with regards to proper training and roadmap of obtaining ISO 22000: 2018 Certification. The ISO 22000: 2018 Certification plays a key role in identifying and controlling hazards related to food safety. Obtaining such certificate will provide a systematic method for analyzing food-manufacturing practices, elimination of possible sources of contamination, and critical plans to prevent unsafe food from reaching the consumers. Clients can avail our services of obtaining ISO 22000: 2018 Certification at reasonable market prices.

Key Elements :

  • Interactive communication
  • System management
  • Control of food safety hazards through pre-requisite programs and HACCP plans
  • Continual improvement and updating of the food safety management system

 

Benefits :

  • ISO 22000: 2018 is a truly international standard suitable for any business in the entire food chain, including inter-related organizations such as producers of equipment, packaging material, cleaning agents, additives and ingredients
  • A major resulting benefit is that ISO 22000: 2018 will make it easier for organizations worldwide to implement the Codex HACCP (Hazard Analysis and Critical Control Point) system for food hygiene in a harmonized way, which does not vary with the country or food product concerned

  • An auditable standard with clear requirements which provides a framework for third-party certification

  • Suitable for regulators

  • Allows organization within the food chain to demonstrate their commitment to food safety

  • Improved internal and external communication

  • Ability to show control of known food hazards

  • Continuous improvement of an organization's food safety management system

  • The structure aligns with the management system clauses of ISO 9001 and ISO 14001

  • Enables communication about hazards with partners in the supply chain

  • System approach, rather than product approach

  • Applicable to all organizations in the global food supply chain

  • Systematic management of prerequisite programmes increased due diligence

  • Dynamic communication on food safety issues with suppliers, customers, regulators and other interested parties

  • Provides potential for harmonization of national standards

  • Covers the majority of the requirements of the current retailer food safety standards

  • Complies with the Codex HACCP principles

  • Provides communication of HACCP concepts internationally

  • A systematic and proactive approach to identification of food safety hazards and development and implementation of control measures

  • Resource optimization – internally and along the food chain

  • All control measures are subjected to hazard analysis

  • Better planning - less post process verification

  • Improved documentation

  • Better product image

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FSSAI Certification

If you are operating in the Food and Beverage Industry of India and seek to get FSSAI Certification from the Food Safety and Standards Authority of India, then look no further than Progressive ISO Certification India Private Limited. We are a Bhopal (Madhya Pradesh) based company having specialization in assisting clients to obtain FSSAI certification for their F&B operations in a legitimate manner. Our learned professionals make it sure that the clients face the least hassles in the FSSAI Certification procurement process.

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NABH Certification

Progressive ISO Certification India Private Limited is a Bhopal (Madhya Pradesh) based company that helps organizations acquire NABH Certification from the competent authority. It is one of the essential certifications in the healthcare industry that exhibits a hospital’s commitment to continuous improvements as well as for quality care. If you are a hospital owner and looking to attain this certification then get in touch with is now. We are backed by a team of professionals, who have great knowledge about the NABH certifications.

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ISO IEC 27001-2013 Certification

The ISO IEC 27001: 2013 Certification, acquired by most organizations, ensures the selection of appropriate and adequate security controls that protect the company’s information assets. This certification specifies the requirements for establishing, operating, and monitoring the security system within the context of the organization's overall business risk. Our professionals are proficient in every aspect of ISO IEC 27001: 2013 Certification and are able to the keep a watch on the size of your organization, the skills of working staff and the networking and data sharing system prevalent in the office. We are capable of successfully training and obtaining ISO IEC 27001: 2013 Certification within the postulated time.

 

ISO/IEC 27001:2013 is intended to be suitable for several different types of use, including the following :

  • Use within organizations to formulate security requirements and objectives

  • Use within organizations as a way to ensure that security risks are cost effectively managed

  • Use within organizations to ensure compliance with laws and regulations

  • Use within an organization as a process framework for the implementation and management of controls to ensure that the specific security objectives of an organization are met

  • Definition of new information security management process

  • Identification and clarification of existing information security management processes

  • Use by the management of organizations to determine the status of information security management activities

  • Use by the internal and external auditors of organizations to determine the degree of compliance with the policies, directives and standards adopted by an organization

  • Use by organizations to provide relevant information about information security policies, directives, standards and procedures to trading partners and other organizations with whom they interact for operational or commercial reasons.

  • Implementation of business-enabling information security.

  • Use by organizations to provide relevant information about information security to customers.

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GMP Compliance Certification

We are widely acknowledged for offering excellent GMP Compliance Certification Services to all the clients. The GMP Compliance Certification helps in improving brand value in the market and hence, it should be there with a company. In addition to this, The GMP Certification gives an assurance to the buyers that your product is safe and correct. We have an experienced staff that guide you all from the start till the end to acquire this certification. You just have to give us a call and rest we will take good care to get you the same.

Benefits of GMP Certification :

  • Improves brand value or image in the market
  • Provide guideline on how to produce safe and quality products.
  • Develops customer satisfaction by deliver the safe and quality product and services.
  • Develops motivation and team work between the employees of the organization.


Process to get the GMP Certification :

  • Application : This is the first step to get the GMP certification, the application covers some basic information of the company. The certification body must accept the application and needs to b record or maintain all the information on the GMP database.
  • Review of Application : The application received shall be reviewed by the team to ensure that the compliance requirement have been fulfilled.
  • Quote and Agreement : After the review of documents we provide the price quotation to the client and performs the Gap Analysis to cover all the clauses and section of the quality standards and Gap Analysis is done to check the Gap between companies planned things and achieved things.
  • Documentation Review : Check the document of the organization to ensure that the documentation fulfilled the compliance requirement.


Stage - 1

  • Audit : Evaluate your organizations documented procedure and policies against the compliance requirement.
  • Review : Review the documentation of your management system to ensure that the compliance requirement have been contented.
  • Corrective Action : Corrective action is deal with the non-conformity. It has taken when the non-conformity occurs.
  • Verification : Verify the documentation of the organization as per the standard requirements.


Stage - 2

  • Audit : In stage-2 audit, the auditor verifies that the organization implement according to its documentation and if the auditor of certification body identifies the non-conformities then the auditor give the opportunity to correct the non-conformities.
  • Review : Review the implementation process according to the organizations document.
  • Corrective Action : If there is any non-conformity occurs then the corrective action has been taken.
  • Verification : Verify work instruction and implementation process are being followed by your employees.
  • Granting of Certification : The Certification Body will issue a certificate of compliance, which is valid for three years.
  • Surveillance Audit : Surveillance audit conduct to ensure that the organization meets the requirements of the management system. Surveillance audit must be performed in every six month or one year from the date of issued certificate.
  • Re-Certification : Re-certification is the process, which is done at the end of three years period.
  • Review : Review the documentation and implementation process of your management system to ensure that the compliance requirement have been contented.
  • Corrective Action : Recheck the non-conformity, if any other problem occurs then CB give the opportunity to the organization to resolve the non-conformity.
  • Verification : Compare the documentation of the organization with the compliance requirement
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Iso Certifications Services

Iso 9001:2008rniso 9001 is a 'generic' standard and is applicable to all organizations irrespective of its size, product, location & whether private / public / government. rnCertification is a internationally recognized quality management systems. Iso 9001:2008 clearly demonstrates the organizations ability to meet customer requirement(s), and commitment to continual improvement. rnAdvantagesrnrn customers are benefited as they receive products & services conforming to requirements. rn owners & investors benefit by increased return on investment, improved operational results, increased market share, increased profile. rn people in the organization benefit through better working conditions, increased job satisfaction helps maintaining high morale. rn society benefits through fulfillment of legal and regulatory requirements, improved health and safety, reduced environmental impact. rnrnquality management system standardsrnthe international organization for standardization has published a family of standards for quality management systems, and is administered by accreditation bodies through certification bodies. They arernrn iso 9000 qms - fundamentals & vocabularyrn iso 9001 qms - requirementsrn iso 9004 - guidelines for performance improvernrnenvironmental management system standardrniso 14001:2004 environmental management system standard helps an organization to minimize the effect of its processes which negatively affect the environment (air, water or land) and comply with applicable regulatory and statutory requirementsrncertification to iso 14001:2004 demonstrates of the organization's earnestness and commitment to environmental performance. rnIso for environment management systems is based upon iso 9000 family of standards. rnBenefitsrnrn reduction of waste hence cost savings. rn improved overall performance & efficiencyrn better public perception of the organization to improved sales. rn reduction of impact of your activities, leading to more community support. rnrnoccupational health and safety assessment seriesrnohsas 18001: 2009 occupational health and safety management systems - specificationsrnthis standard prescribes requirements for an oh&sms to enable an organization to formulate its policies and objectives to protect its employees and others, whose health and safety may be affected by the activities of the organization. rnThe extent of application depends on nature of activities, complexity of its operations. rnIntegrated management systemrniso 9001, iso 14001 and ohsas 18001 have common elements between them. These can be integrated to a single, management system or a combination of the above. Audit of joint systems is available and best cost effective method for some companies. rnIntegrated system not only help an organizations internally, by reducing duplication and providing a centralized document control system, results in cost benefits in third party audits. rnrnfood safety management systemsrniso 22000:2005 -"food safety management systems - requirements for any organization in food industry", rniso 22000:2005 is a new international standards designed to ensure the safety of food supply chains worldwide while applying haccp programe, in addition to the harmonized applicable qms and prerequisite program. rnIso 22000 specifies a food safety management system that include interactive communication between supplier and producers and customers. It answered the growing demand for the certification of suppliers and gives more attention to quality aspects. rnThe standard is applicable to all organizations directly or indirectly involved in one of the stages, related to the food chain, intending implementing a management system that would guarantee food safety for consumers. rnVarious companies, from seed producers, meat or milk processors, etc., to food transportation companies and even retailers, private food unit or equipment manufactures for the food industry can successfully apply iso 22000:2005, "food safety management systems - requirements for any organization in food industry", rnrniso 27001rniso/iec 27001, part of the growing iso/iec 27000 series of standards, is an information security management system (isms) standard published in october 2005 by the international organization of standardization (iso) and the international electro technical commission (iec). Its full name is iso/iec 27001:2005 - information technology.- security techniques. rnIsms - requirements but it is commonly known as 'iso 27001'. Iso/iec 27001 certification process usually involves a three stage audit process. rnStage 1: is a "table top" review of the existence and completeness of key documentation such as the (soa) and risk treatment plan (rtp)rnstage 2: is a detailed, in depth audit involving testing the existence and effectiveness of the information security control stated in the soa and rtp, as well as their supporting documentation. rnStage 3: is a follow-up reassessment audit to confirm that a previously - certified organization remains in compliance with the standard certification maintenance involves periodic reviews and re-assessments to confirm that the isms continues to operate as specified and intended. rnIso/iec 27001:2005 covers all types of organization [e.g. Commercial enterprises, government agencies, not for profit organizations). Iso/iec - 27001:2005 specified the requirements for establishing, implementing, operating, and monitoring, reviewing, maintaining system within the context of the organization's overall business risk. It specifies requirements for the implementation of security controls customized to the needs of individual organizations (or) parts thereof. rnIso/iec 27001:2005 is designed to ensure the selection of adequate and proportionate security controls that protect information assets and give confidence to interested parties. rnIso/iec 27001:2005 is intended to be suitable for several different types of use, including the following:rnrn use within organizations to formulate security requirements and objectivesrn use within organizations as a way to ensure that security risks are cost effectively managedrn use within organizations to ensure compliance with laws and regulationsrn use within an organizations as a process framework for the implementation and management of controls to ensure that the specific security objectives of an organization are metrn definition of new information security management processrn identification and clarification of existing information security management processesrn use by the management of organizations to determine the status of information security management activitiesrn use by the internal and external auditors of organizations to determine the degree of compliance with the policies, directives and standards adopted by an organizationrn use by organizations to provide relevant information about information security policies, directives, standards and procedures to trading partners and other organizations with whom they interact for operational or commercial reasonsrn implementation of business-enabling information security. rn use by organizations to provide relevant information about information security to customers. rnrnrnmanagement system for the design and manufacture of medical devicesrniso 13485:2003 represents the requirements for a comprehensive management system for the design and manufacture of medical devices. All requirements of this international standard are specific to organizations providing medical devices, regardless of the type or size of the organization. This standard supersedes earlier documents such as en 46001 and en 46002 (both 1997), the iso 13485 published in 1996 and iso 13488 (1996). Iso 13485:2003 is a quality system standard designed specifically for medical device companies. The standard is applied by most class ii and iii (plus class iv in canada) medical device manufacturers to meet the quality system requirements of europe, canada, australia, japan and other parts of the world. rnCompliance with iso 9001:2008 is often seen as the first step in achieving compliance with iso 13485:2003, which is based on the iso 9001:2008 process model, suggests that the application and management of a system of processes is an effective way to ensure good quality management. All requirements of this international standard are specific to organizations providing medical devices, regardless of the type or size of the organization. rnIso 13485 in part designed to produce a management system that facilitates compliance to the requirements of customers and various global regulators. While being certified to iso13485 does not fulfill the requirements of either the fda or foreign regulators, the certification aligns an organization's management system to the requirements of the fda's quality system regulation (qsr) requirements as well as many other regulatory requirements found throughout the world. Therefore, iso13485 certification serves to create a management system that can be thought of as a framework on which to build compliance to various regulatory and customer requirements. rnThe iso 13485 standard supplements iso 9001 and has many of the same requirements. However, there are additional requirements for process control, design control, retention of records, accountability, traceability, customer satisfaction and more. Individual countries such as canada and japan have additional requirements necessary to meet their specific regulations. Iso 13485 certification is not accepted by the us fda, although it shares many of the same characteristics as fda good manufacturing practice (gmp). rnThough based on iso 9001, iso13485 removes 9001's emphasis on continual improvement and customer satisfaction. In its place is an emphasis on meeting regulatory as well as customer requirements, risk management and maintaining effective processes, namely the processes specific to the safe design, manufacture and distribution of medical devices. rnCe markingrnthe european union is keen to ensure that all products entering and used within the union are such as not to impose a threat to consumers or the environment. rnThe european community aims to ensure that industrial products made available on the community market respect a high level of protection of public interests such as health and safety, protection of consumers and the environment. rnA common indication of a product's fitness for placement within the community is the affixing of a ce mark. rnCe markingrnrnrnapplicationrnthe client can forward the application to pcs with organization details, manufacturing setup, etc., rnreadiness reviewrna top level review will be conducted by the pcs at the manufacturer's premises. This is necessary because of the combined complexity of the ce marking and authorised representative processes. It can be likened to a stage one review. The readiness review will indicate to the manufacturer the likelihood of achieving ce mark status for their product, the probable timescale and whether or not specialist help may be necessary. Manufacturers should note that a common circumstance is that products will have developed during a period of several years. Moreover, the level of sophistication of a manufacturer's management practices and personnel will have developed in similar manner. Data regarding the excellence of the design of the product may not therefore be currently available. Often the requirement 'in the early days' was either non-existent or unappreciated. Nonetheless, today's european community requirement is that products should posses known qualities and data relating to their health and safety properties. Collating such data may not be an easy or rapid task and for this reason a readiness review is considered essential in order to ascertain realistic project milestones and costs for ce marking. rnTechnical construction filernthe manufacturer must prepare a technical construction file for the products intended for the european market. The file will contain evidence as to why the product, when installed, maintained and used in accordance with specified instructions, will not present an unreasonable hazard or risk to health and safety or to the environment. The technical construction file will contain product information, especially relating to the design evaluation and the risks and hazards evaluated. It will also address the manufacturing capability of the manufacturer and its ability to achieve the quality of design in a manufacturing environment. Typically a certificated quality management system such as iso 9001 will be of assistance in demonstrating this. However iso 9001 certification not necessarily, on its own, contain sufficient evidence of safeguards in the potential of design. Other information may be necessary and should be expected to be forthcoming on most occasions. Typically this will be information and data arising from the manufacturing process. rnProduct releasernpcs does this in five stages:-rnrn stage one, on site document review. rn stage two, on-site assessment. rn stage three, ce mark certification. This is done at the pcs premises. rn stage four, product release. (i.e. Issue of appropriate certificates). rn surveillance. Typically this would be on a two year cycle but may be more frequent if necessary. rnrnit is the responsibility of the manufacture to advise the pcs of such changes in business structure, product design, or manufacturing systems that could impact upon the basic characteristics, fit, form or function of the product. Failure to advice of relevant changes may invalidate their ce mark status and relationship with the authorized representative. rnAssignmentrnthe assignment process is that whereby the pcs assigns ascb(e) to the manufacturer as their authorised representative in europe. Notification to ascb(e) has to be done within a defined period of time. Reference numbers are allocated and where not previously performed, all technical documentation and documentation pertaining to stages three and four, shall be put into electronic format and copies submitted to ascb(e) for secure and confidential retention in europe. rnDocuments expected to be submitted are as follows:rnrn technical construction filern declaration of conformityrn release certificaternrnacceptancernfollowing receipt of pcs submission, ascb(e) reviews documentation as appropriate and retains registries within europe of the ce marked products. A register is maintained for public access subject to the provisions of legislation requiring data security. rnAccreditationsrnpcs is striking a balance between providing popular accreditation to its customers at the same time providing cost effective service. rnPcs is accredited with accreditation bodies for certifying agencies, united kingdom (ascb (e)). rnPcs as required can organize other accreditation like anab, ansi-asq national accrediation board, us;dutch accreditation council, rva netherland; dar, t.g.a gmph german; & nabcb (national accreditation board for certifying bodies)india; through respective accredited cb's.
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Iso Certifications, Trade Mark

We Provide ISO certifications, trade mark.
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Iso Certification Services

We Provide Iso Certification Services.
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Iso Certifications Services

We provide Iso Certifications Services.
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  • Mr. Abhishek (Progressive Certification Services)
  • F – 4, HIG, Golden Valley Apartment, Opposite Sagar Complex, Kolar Road, Bhopal, Madhya Pradesh 462016, India
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