ISO 9001:2015 (Quality Management System). CDG is a leading ISO 9001 certification company of India. Our ISO 9001 certification service are accredited. ISO 9001 certification is the best way to declare quality of your working system among your customers and other stake holders. ISO 9001:2015 certification increases trust of your organization among different concern groups. ISO 9001:2015 is the latest quality management system standard. It was published on 15th September 2015. ISO 9001 standard was prepared by Technical Committee ISO/TC 176. This fourth edition cancels and replaces the third edition (ISO 9001:2000 standard), which has been amended to clarify points in the text and to enhance compatibility with ISO 14001:2015. ISO 9001 standard provides a set of standardized requirements for a quality management system, regardless of activities of the organization, its size, or whether it is in the private or public sector. All requirements of ISO 9001:2015 Standard are generic and are intended to be applicable to all organizations, regardless of type, size and product/services provided by the organization. It is not the intent of ISO 9001 Standard to imply uniformity in the structure of quality management systems or uniformity of documentation. Benefits of ISO 9001 Certifiction: - ISO 9001 certification enhance customer satisfaction by meeting customer requirements. - ISO certification enhance function efficiency of an organization - ISO 9001:2015 implementations help to manage the resources effectively - Once you obtained ISO 9001 certificate it creates path to improve the processes continually - ISO 9001:2015 certificate is now required in majority of goverenment tenders - ISO 9001:2015 certification is Today passport of your organization for overseas business.
* ISO 9001 certification enhance customer satisfaction by meeting customer requirements. You become able to provide right products or services. * ISO certification enhance function efficiency of an organization. As you develope SOP's & Work Instruction for all your processes. * ISO 9001:2015 implementations help to manage the resources effectively, as you become able to utilise all your resources to its maximum extent. * Once you obtained ISO 9001 certificate it creates path to improve the processes continually. * ISO 9001:2015 certificate is now required in majority of goverenment tenders. * ISO 9001:2015 certification is Today passport of your organization for overseas business
* Apply for ISO 9001:2015 certification on our decided ISO 9001 application form (Doc CDG 003). & send your ISO application to CDG in hard copy or soft copy. * CDG will review your application & generate a quotation. This quotation will include all cost of ISO 9001 certification. You need to accept the quote & pay ISO certification fee. * CDG office will send you stage stage 1 ISO audit plan & subsequently stage-1 ISO audit will be conducted as per plan. * After successful stage 1 audit & closure of stage 1 non conformities (if any) CDG will send you stage 2 ISO 9001 audit plan & stage 2 audit will be conducted accordingly. * After successful stage 2 audit & closure of stage 2 non conformities (if any), ISO auditor will recommend your organization for issuance of ISO 9001 certificate. * Subsequently ISO 9001 certification decision is taken by CDG as per it’s defined procedures & an ISO 9001:2015 certificate is issued for your organization. * Every year a surveillance audit is conducted to ensure continued adherence of your quality management system to the requirements of ISO 9001 standard.
In the year 1979 a new standard was proposed based on BS 5750. * In the year 1987 ISO published it’s 1st edition of ISO 9001 standard (for quality assurance in design, development, production, installation, and servicing including the creation of new products), along with ISO 9002 (QMS for organizations not doing design & development without covering the creation of new products.), ISO 9003 (covered only the final inspection of finished product). * In the year 1994 a limited revision standard ISO 9001:1994 was published. * In the year 2000 a major revision was done withdrawing ISO 9002, ISO 9003 standards & ISO came with a common standard for every one i.e. ISO 9001:2000. * In the year 2008 a minor amendment was done & new standard was known as ISO 9001:2008. * In the year 2015 ISO made major changes in the structure & approach of standard and the new & latest standard is known as ISO 9001:2015
New standard ISO 9001 2015 has been published with many core changes. Few new requirements have been introduced that was not there in ISO 9001:2008 standard. Some major changes are as follows:
Structural changes – The old standard (ISO 9001:2008) had 5 main sections / clauses (i.e. Clause 4 to clause 8) while in new standard (ISO 9001:2015) there are main 7 sections i.e. Clause 4 to clause 10). The new standard is more prepared for integration.
Context – Now while establishing your quality management system, you have to decide context of your organization. Now you have to focus on needs & expectations of interested parties. The new standard ISO 9001:2015 wants you to consider external & internal issues which are relevant to your QMS.
Documented Information – In new standard ISO 9001:2015 it is not mandatory to have documented procedures or a quality manual. Unlike old standard terms ‘document’& ‘Records has been eliminated & now both are known as ‘documented information’
Risk Based emphasis - The new standard ISO 9001:2015 wants you to identify & address risks & opportunities that can affect your product & service compliances which will result into increased customer satisfaction.
Exclusions & Requirements – In old standard ISO 9001:2008 exclusion was limited to clause / section 7 only but now in ISO 9001:2015 the same concept can be applied to any clause / section if it is justified.
Objects, Outputs, Products and Services – ‘Object’ is a new term in ISO 9001:2015 which means anything conceivable or perceivable. What was used to be called ‘product ‘in old standard (ISO 9001:2008) is now called ‘Output ‘in the new standard. Now both product & services are thought of as ‘outputs’.
ISO 9001:2015 (Quality Management System) CDG is a leading ISO 9001 certification company of India. We provide accredited ISO 9001:2015 certification services. ISO 9001 certification is the best way to declare quality of your working system among your customers and other stake holders. ISO 9001.
ISO 14001:2015 is the most popular certification standard for EMS (environmental management system) worldwide. Your ISO 14001 certificate ensure your customers, stakeholders & environmental authorities that you have assessed impact of your activities over your surroundings & have taken proper measure to eliminate or minimise negative impact. ISO 14001 certification provides you a tool to control all your processes with environmental viewpoint.
CDG is a leading EMS ISO 14001 certification company worldwide, Our EMS audit ensures that you strictly meet requirements of ISO 14001 standard & statutory/regulatory environmental norms applicable on your business as well. In a sense ISO 14001 certification also strengthen you CSR activities as you act for betterment of your immediate environment. Our ISO 14001 certification process is result oriented & our EMS ISO 14001 auditor focus on practical implementation of ISO 14001 requirements. All our EMS auditors are experts of environmental management issues & have long working experience in the same domain.
* ISO 14001 ensures that all processes has been made environment friendly & hence your processes gets improved for maximum utilisation of resources. * Your organisation gets ready for any kind of statutory, regulatory or buyers audit related to environmental management system. * As EMS ISO 14001 certificate is issued for better environmental practices, image of your organisation gets improved among your customers & stake holders
Food safety management systems
ISO 22000:2005 is a food safety management for organizations involved in food chain. This standard specifies the requirements for food safety management system where an organization in food chain needs to demonstrate its ability to control the food related hazards. This standard was prepared by Technical Committee ISO/TC 34, Food products. Food safety is related to the presence of food-borne hazards in food at the point of consumption. As the food safety hazards can occur at any stage of the food chain, adequate control throughout the food chain is essential. Thus, food safety is ensured through the combined efforts of all the parties participating in the food chain.
This International Standard specifies the requirements for a food safety management system that combines the following generally recognized key elements to ensure food safety along the food chain, up to the point of final consumption:
* Interactive communication * System management * Prerequisite programmes * HACCP principles.
The main aim of this standard is to harmonize on a global level the requirements for food safety management for businesses within the food chain. It is particularly intended for application by organizations that seek a more focused, coherent and integrated food safety management system than is normally required by law. It requires an organization to meet any applicable food safety related statutory and regulatory requirements through its food safety management system.
This International Standard integrates the principles of the Hazard Analysis and Critical Control Point (HACCP) system and application steps developed by the Codex Alimentarius Commission. By means of auditable requirements, it combines the HACCP plan with prerequisite programmes (PRPs). Hazard analysis is the key to an effective food safety management system, since conducting a hazard analysis assists in organizing the knowledge required to establish an effective combination of control measures.
ISO 13485:2016 is a specific certification standard for medical device industry. ISO 13485 certification fulfils your needs related to production control, quality management, regulatory compliances & specific needs related to production of a particular medical device. ISO 13485 is basically a QMS for medical device industry that is why it is also known as ‘MD QMS’. ISO 13485 certificate satisfies potential customers & stakeholders with the fact that a device has been manufactured following internationally recognised ISO 13485 standard. ISO 13485 audit by CDG ensures that an organisation meets all guideline of ISO 13485:2016 & this is the reason why CDG is an industry trusted ISO 13485 certification company. Our ISO 13485 certification process is result oriented & customer focused. We are a pioneer ISO 13485 certification body of India. All requirements of ISO 13485 are specific to organizations providing medical devices, regardless of the type or size of the organization
* ISO 13485 improves performance or products & processes of a medical device company. * ISO 13485 certificate is universally recognized & it covers regulatory & statutory norms of most of countries, your product gets an expended market access. * ISO 13485 works as a brand ambassador of your medical device hence your sales & marketing cost will reduce. * ISO 13485 certification gives faith to your customers that device is safe for use & it meets requirements of most of recognized technical standards related to medical device
* Apply for ISO 13485:2016 certificate by submitting filled in ISO 13485 application form (Soft copy or hard copy). * Application form will be reviewed by our ISO 13485 auditor / expert & if accepted a quotation for ISO 13485 certification will be issued. * Upon submission of ISO 13485 certification fee, we will send you ISO 13485 audit plan (stage-1) & subsequently audit will be conducted. * After successful stage-1 audit closure of NC’s (if any), CDG will send you stage -2 ISO 13485 audit plan. After successful audit, auditor will recommend your organization for ISO 13485 certification. * Based on auditor’s recommendation & audit findings CDG’s certification authority will take decision for grant of ISO 13485 certificate
Now ISO 13485:2016 certification standard has come with many changes. Few important changes are as follows-
Flexible – New standard ISO 13485:2016 is more flexible as it allows you to make exclusions in section 6, 7 & 8 if it can be justified while in old standard ISO 13485:2013 exclusion was permissible only in section 7. In this way new standard ISO 13485:2016 is more flexible.
Regulations – In old standard ISO 13485:2013 a QMS had to established based on requirements of the standard & product, while in new version ISO 13485:2006 emphasis has been given on meeting regulatory requirements. Now QMS has to be established encompassing applicable regulatory requirements.
Risk Based Approach – In old version risk analysis approach was applicable to ‘product realization’ only, while in new version ISO 13485:2016 risk based approach is applicable to all processes of QMS
Enhanced Record Keeping – New standard ISO 13485:2016 expects you to keeps record of supplier monitoring, evaluation & re-evaluation. Now privacy has to be maintained in maintaining confidential health information.
Product Realization – New standard ISO 13485:2016 says to establish procedures for storage, handling of products, traceability, measurement & revalidation in addition to requirements of old standard ISO 13485 which required procedure for verification, validation, monitoring, inspection & testing
Training of Users – The new standard ISO 13485:2016 says to educate / train the user about product safety & regulatory norms.
ISO/IEC 27001 specifies requirements for the establishment, implementation, monitoring and review, maintenance and improvement of a management system - an overall management and control framework - for managing an organization's information security risks. It does not mandate specific information security controls but stops at the level of the management system. It is a set of 'best practices' controls - management and systems - that enables you and your organisation demonstrate 'best practices' are implemented and 'continually' improved. The ISO/IEC 27002 2013 standard consists of recommended information security practices.
With ISO 27001 certification from CDG, you can show your clients and partners the level of security and quality of your IT-based business processes. CDG has the expertise to certify information security management systems in accordance with ISO 27001. CDG's ISO 27001 certificate gives a faith to your customers & stakeholders that their information / data is secure with your organisation.
Competitive advantage - As information security is very important for any organisation, ISO 27001 Certification will give you a competitve advantage when you are compared with others.
Demonstrating your capability - You will be able to make a public statement of capability without revealing your security processes.
Minimising risk - Ensures controls are in place to reduce the risk of security threats and to avoid system weaknesses being exploited. Less changes of loss / theft of information.
Compliance with legislation - your organisation comply with legislative requirements related to information security. You also comply with your buyer's information security requirements.
Globally recognised standard: ISO 27001:2013 is the only ISMS standard with global acceptence.
Potential reduction in insurance premiums : As information / data will remain secure so you need not to use your indemnity inssurance to protect interest of your stakeholders.
Security becomes an integral part of business processes : - the As ISO 27001 certification has a information security management system approach, information security becomes part of you processes.
ISO 20000 is the world's first international standard for IT Service Management. ISO/IEC 20000 is an international IT standard that allows companies to demonstrate excellence and prove best practice in IT management. The standard ensures companies can achieve evidence-based benchmarks to continuously improve their delivery of IT services. ISO/IEC 20000 was released in 2011 based on the IT infrastructure library (ITIL®) best practice framework, and updated in 2011.
The standard is intended for organizations who provide managed IT services such as infrastructure and/or applications support; this can be both for external delivery e.g. to clients who have outsourced their IT support, as well as for internal IT groups. A certificate issued by third party registrar to demonstrates that your IT management system has been certified against requirements of ISO 20000 requirements. Implementation of ISO 20000-1 by setting up of internal processes gives confidence to customers about the delivering capability through use of IT infrastructure.
ISO/IEC 20000-1:2011 is the formal specification and defines the requirements for an organization to deliver managed services of an acceptable quality for its customers. The scope includes:
* Requirements for a management system * Planning and implementing service management * Planning and implementing new or changed services * Service delivery process * Relationship processes * Resolution processes * Control processes * Release processes.
- Alignment of information technology services and business strategy.
- Creation of a formal framework for current service improvement projects
- Provides a benchmark type comparison with best practices
- Creates competitive advantage via the promotion of consistent and cost-effective services.
ISO 28000 standards specifies the requirements for a supply chain security management system, linking security management to many other aspects of business management. For organisations working within, or relying on, the logistics industry, certification to the ISO 28000:2007 supply chain management standard provides a valuable framework. It will help minimise the risk of security incidents and so help provide problem-free 'just in time' delivery of goods and supplies. ISO 28000 standard sets in place mechanisms and processes to address security vulnerabilities at strategic and operational levels, as well as establish preventive action plans. ISO 28000 is suitable for all sizes and types of organisation that are involved in purchasing, manufacturing, service, storage, transportation and/or sales processes, and wish to implement and maintain a secure management system for its supply chain.
CDG is at the leading edge of supply chain security management system certification. We have experience of security assessments gained from carrying out audits of many exporters, warehouses & ICD's. Organizations that choose CDG’s ISO 28000 certification can demonstrate that they are contributing significantly to supply chain security.
* Establish, implement, maintain and improve a supply chain security management system. * Assure conformance with supply chain security management policy * Demonstrate conformance to requirements of supply chain security management * Educate / train your vendors / subcontractors in supply chain. * Conduct internal security audit & record audit findings. Develope system of continuous monitoring of security arrangements & recording incidemnces of security breaches
* Allows security to be managed as a process so that the effectiveness of security
management can be measured and improved. * Allows management to focus resources and efforts on areas with high-risk concerns (through a security risk assessment). * Allows management to benchmark its security management efforts with international standards. * Demonstrates to stakeholders the commitment to enforce
OHSAS 18001:2007 is the International Occupational Health and Safety Management Standard.. OHSAS 18001 provides a framework to the effective management of OH&S including compliance with the legislation that applies to your activities and identified hazards. OHSAS 18001 sets requirements for monitoring and improving safety in the workplace. In addition to the OHSAS 18001 specifications, there is a guidance document known as OHSAS 18002:2000 Occupational Health and Safety Management Systems Guidelines for the implementation of OHSAS 18001. The standard is applicable to any organisation that wishes to eliminate or minimize risk to employees and other stakeholders who may be exposed to OH&S risks associated with its activities.
The certification for occupational health and safety management systems that is globally recognized is the OHSAS 18001 certification. It was developed to bridge the gap in employee welfare criteria where no third-party international standard existed. CDG's OHSAS 18001 certificate is recognised globaly.
* Hazard identification, danger assessment and ways to control these. * An OHSAS (occupational health & safety) management program. * Structure and responsibility for occupational health and safety measures. * OHSAS training and awareness program. * Communication to internal and external parties regarding occrpationl health & safety.
* Operational control to avoid chances of accidents & incidents. * Emergency watchfulness and prompt response. * Performance measurement, monitoring and skill enhancement
* Increases employees' safety awareness and motivation. * Ensure that you fulfil statutory and official health and safety requirements. * Prevent accidents & incidents. * Reduced risk to employees, customers and suppliers. * Reduction in the costs associated with accidents at work. * Enhanced staff morale and motivation. * Demonstration of legal and regulatory compliance
HACCP stands for - Hazard Analysis Critical Control Point. HACCP system that includes a series of procedures for process control and sensitive points in the food chain, with the ultimate aim that the consumer uses the food in the state and in a manner that will be safe for his health. HACCP system in seventies became recognized as an international standard for food production. The certification process for HACCP is similar to any other certification schemes.
* Preparation of HACCP Team : You need to invlove all concerned employess in your organisation & prepare a HACCP team- Development of HACCP plan : Based on nature of business & potential risk to food you need to develope a HACCP Plan * Implementation of HACCP plan : You need to implement HACCP system as per your HACCP plan allocating proper responsibilities to your HACCP team members * HACCP certification audit by an international HACCP certification body like CDG * Maintenance and monitoring of the HACCP system : After certification you need to follow HACCP food safety system continuously, CDG will also monitor your food safety syste through regular HACCP audits .
* The implementation of hazard analysis. * Determine Critical Control Points (CCP). For each risk identified. * Establishing critical limits, maximal and / or minimum value, by which biological, chemical and physical hazards in order to control the pedagogical prevention. * Determination of procedures / processes for monitoring CCPs * Determination of corrective measures in case the monitoring shows that the CCP is not within the critical limits. * Establish procedures / processes for verification and certification procedures and the HACCP
system is effective and it works well. * The verification activities should be included authorized persons employed in production, the HACCP team. * The establishment and effective management of records and documents
HACCP stands for - Hazard Analysis Critical Control Points. HACCP system that includes a series of procedures for process control and sensitive points in the food chain, with the ultimate aim that the consumer uses the food in the state and in a manner that will be safe for his health.
ISO 50001 gives organizations the requirements for energy management systems (EnMS). ISO 50001 certification is based on the management system model that is already understood and implemented by organizations worldwide. ISO 50001 will provide public and private sector organizations with management strategies to increase energy efficiency, reduce costs and improve energy performance. Like all ISO management system standards, ISO 50001 has been designed for implementation by any organization, whatever its size or nature of business / activities, regardless of its geographical location. This International Standard specifies requirements of an energy management system (EnMS) for an organization to develop and implement an energy policy, establish objectives, targets, and action plans, which take into account legal requirements and information related to significant energy use. CDG is a leading ISO 50001 certification company in India & our ISO 50001 certificate is recognized worldwide. Contact CDG for ISO 50001 audit & certification services.
ISO 50001:2011 standard is also known as energy management system. ISO 50001 certification provides a framework for using energy efficiently.
TS 16949 is the International Quality Management Standard specifically written by the Automotive Industry. ISO/TS 16949:2009 is an ISO Technical Specification which aligns existing US, German, French and Italian automotive quality system standards within the global automotive industry. ISO/TS 16949:2009 specifies the quality system requirements for the design/ development, production, installation and servicing of automotive-related products. ISO/TS 16949:2009, based on the eight quality management principle, specifies the quality system requirements for the design/ development, production, installation and servicing of automotive-related products. It also creates an implementation framework for customer specific requirements, and includes clear requirements for development processes, and techniques to prevent problems in the earliest possible stage of product development. CDG is leading ISO TS 16949 certification company & our ISO ISO TS 16949 certificate is recognised worldwide by big automobile gaints.
TS 16949 certificate provide enhanced customer confidence and satisfaction, which in turn can lead to increased business opportunities - TS 16949 certification gives you a global recognition as a reputable supplier - TS 16949:2009 certification is recognized and accepted throughout the automotive supply chain as an industry benchmark - Commercial advantage confirming your efficiency and guaranteeing the quality of your processes and the product.
Road accidents belong to the most common causes of injury and death. The analysis of road accident data 2015 reveals that about 1,374 accidents and 400 deaths take place every day on Indian roads which has increased by 2.5% in comparison to 2014. India is a signatory to Brasilia Declaration and is committed to reduce the number of road accidents and fatalities by 50 per cent by 2020. To achieve this goal ISO 39001:2012 certification can play a great role.
ISO 39001:2012 standard specifies requirements for a road traffic safety (RTS) management system to enable an organization that interacts with the road traffic system to reduce death and serious injuries related to road traffic crashes which it can influence. The requirements in ISO 39001:2012 include development and implementation of an appropriate RTS policy, development of RTS objectives and action plans, which take into account legal and other requirements to which the organization subscribes, and information about elements and criteria related to RTS that the organization identifies as those which it can control and those which it can influence.
ISO 39001 "Road traffic safety (RTS) management systems" is an ISO standard for a management system (similar to ISO 9000) for road traffic safety. The implementation of the standard is intended to enable organizations to improve their traffic safety and to reduce the number of persons killed or severely injured.
CDG’s ISO 39001 sets out the minimum requirements for a Road Traffic Safety Management System. Validate that you are committed to implementing and maintaining a Road Traffic Safety Management system by getting certified to CDG's ISO 39001. CDG is an experienced service provider for ISO 39001 certification and supports you with comprehensive services tailored to your needs.
Which Companies Require ISO 39001 Certification ?
RTSM - Road Traffic Safety Management is relevant to all organizations, regardless of business type or scale.
Companies which use motor vehicles (trucks) for transportation of goods or provide business services.
Companies providing transportation services: transportation of goods or passengers (i.e. truck, bus, taxi companies).
Organizations / Institutions involved in establishing Road Traffic Safety laws (i.e. governments, local public organizations).
Companies involved in the designing, manufacturing, maintaining, and inspecting of motor vehicles (i.e. Automobile manufactures).
Companies / Organizations and businesses having parking facilities (i.e. supermarket, parking management companies).
Organizations involved in the designing, building, operating and maintaining of roads (i.e. Road authorities).
Organizations involved in providing emergency medical care (i.e. emergency medical centers, hospitals, Ambulance Services).
Benefits of ISO 39001 Certification
ISO/TS 29001:2010 defines the quality management system for product and service supply organizations for the petroleum, petrochemical and natural gas industries. The ISO/TS 29001:2010 was developed as the result of cooperation between the American Petroleum Institute (API) and ISO technical committee ISO/TC 67.
The ISO/TS 29001:2010 standard is based on ISO 9001, and includes supplementary requirements highlighting defect prevention and the reduction of deviation and waste from service providers. All requirements of ISO/TS 29001 are generic and are intended to be applicable to all organizations, regardless of type, size and product provided.
ISO 29001 certification is for organizations involved in exploration, production, pipelines and transport, refining of petroleum and natural gas and those that provide technical and support services to these industries. ISO 29001 specification is also applicable to manufacturers and purchasers of oil and gas industry equipment can also use this technical specification.
Benefits of 29001 Certification:
CDG’s well experienced auditors ensure effective sector-specific QMS (ISO 29001) which provides additional assurance to the customers of our certified clients. ISO/TS 29001 is expected to result in „increased international acceptance of time-tested sector-specific quality system requirements on a broad scale for the worldwide oil and gas industry. Implementing ISO/TS 29001 with CDG demonstrates your organization’s commitment to quality. It covers your systems and processes and shows you care about your personnel and the public. CDG’s auditing staff is uniquely qualified to be a value-added part of your journey to develop your ISO 29001 quality system.
Call today for more information on ISO/TS 29001 at 1800-843-0018 or request at quote at the top of this page.
Bribery is one of the world’s most destructive and challenging issues. With over US$ 1 trillion paid in bribes each year*, the consequences are catastrophic, reducing quality of life, increasing poverty and eroding public trust. •ISO 37001 is an anti-bribery management system standard published in October 2016. •It is designed to help an organization establish, implement, maintain, and improve an anti-bribery compliance program. It includes a series of measures and controls that represent global anti-bribery good practice. The measures required by ISO 37001 are designed to be integrated with existing management processes and controls. It follows the common high-level structure for ISO management system standards, for easy integration with, for example, ISO 9001. New or enhanced measures can be integrated into existing systems.
Who can use this Standard?
The standard is flexible and can be adapted to a wide range of organizations, including:
•Small & medium sized enterprises (SMEs)
•Public and private sector organizations
•Non-governmental organizations (NGOs)
The standard can be used by organizations in any country.
What does the ISO 37001 standard require?
The organization must implement a series of measures and controls in a reasonable and proportionate manner to help prevent, detect, and deal with bribery, including:
•Management leadership, commitment and responsibility
•Personnel controls and training
•Due diligence on projects and business associates
•Financial, commercial and contractual controls
•Reporting, monitoring, investigation and review
•Corrective action and continual improvement
ISO 37001 is a requirements standard, making it capable of independent certification. CDG is a world leading organisation for ISO 37001 certification. Contact CDG for ISO 37001 certification services.
ISO 22716:2007 gives guidelines for the production, control, storage and shipment of cosmetic products. These guidelines cover the quality aspects of the product & this standard is recognised by International Cooperation on Cosmetics Regulation (ICCR), Food & Drug Administration (FDA) and the European Committee for Standardisation (CEN). ISO 22716 introduces a management systems approach to documenting and regulating the production, control, storage, and shipment of cosmetic products. FDA has declared elements of ISO 22716, as appropriate, and consistent with FDA regulations. Cosmetics Good Manufacturing Practices are a set of hands-on advice, operational rules and organizational guidelines that focus on human, technical and administrative factors affecting product quality.
ISO 22716 certification is the way to demonstrate compliance with GMP. ISO 22716 provides Cosmetics Good Manufacturing Practices (GMP) guidelines, rules and advice that underpin the European Union’s new Regulation (EC) No. 1223/2009. The term ‘Cosmetics GMP’ is commonly used to refer to ISO 22716:2007. CDG’s accredited ISO 22716 certification audits complements an organization’s commitment to quality and consistency in the cosmetic industry.
ISO 22301:2012 specifies requirements to plan, establish, implement, operate, monitor, review, maintain and continually improve a documented management system to protect against, reduce the likelihood of occurrence, prepare for, respond to, and recover from disruptive incidents when they arise.
The requirements specified in ISO 22301:2012 are generic and intended to be applicable to all organizations, or parts thereof, regardless of type, size and nature of the organization. The extent of application of these requirements depends on the organization's operating environment and complexity. This standard addresses business continuity management to contribute making organizations in both public and private sectors more resilient. It is intended to ensure that organizations can respond and continue its operations. ISO 22301:2012 - Business continuity management systems will help your organisation regardless of size, location, or activity, to be better prepared and more confident to handle unexpected and disruptive incidents. ISO 22301 may be used for third-party certification as well as for self-assessment. To help users get the best out of the Standard, it includes short and concise requirements describing the central elements of BCM. The ISO 22301 standard applies the Plan-Do-Check-Act or PDCA model in the planning, establishment, maintenance and review of a Business Continuity Management System. The ISO 22301 standard requires organizations to determine the scope of the BCMS they intend to implement. ISO 22301: 2012 has been adapted by organizations seeking to demonstrate business continuity processes. The standard replaces the erstwhile BS 25999:2 2007, which now stands replaced. CDG provides certification services for ISO 22301 in all major cities of India & abroad.