What is the difference between iso 13485 and 21 cfr 820?

#WHAT IS THE DIFFERENCE BETWEEN ISO 13485 AND 21 CFR 820? VERIFICATION#

The scope of application is mandatory in the national territory, for all establishments dedicated to the process of medical devices marketed in the country. NOM-241-SSA1-2012, Buenas Practicas de FabricaciГіn para Establecimientos dedicados a la FabricaciГіn de Dispositivos MГ©dicos. Mexico published in Octoa national standard as a Norma Oficial Mexicana (NOM) to control manufacture of medical devices inside the country. This standard adopted by CEN as EN ISO 13485:2012 is harmonized with respect to the European Medical Devices Directive 93/42/EEC. The IMDRF main membership (the regulators) do want to have non-regulators involved without voting rights and in this way they are hoping to get the process and documents completed quicker than under the GHTF system (regulators & non-regulators were equal in voting rights) that worked reasonably well, but somewhat slow. The GHTF has been replaced in the last few years by the International Medical Device Regulatory Forum (IMDRF) and is structured differently from the GHTF as only the regulators, that are primary members of the group, get to make many of the decisions. The GHTF guidelines are slowly becoming universal standards for design, manufacture, export and sales of various medical devices. ISO 13485 is now considered to be inline standard and requirement for medical devices even with ' Global Harmonization Task Force Guidelines' (GHTF). This standard adopted by CEN as EN ISO 13485:2003/AC:2007 is harmonized with respect to the European medical device directives 93/42/EEC, 90/385/EEC and 98/79/EC. Several registrars also act as Notified Body.ДЇor those medical devices requiring the pre-market involvement of a Notified Body, the result of a positive assessment from the Notified Body is the certificate of conformity allowing the CE mark and the permission to sell the medical device in the European Union.ДЄ very careful assessment of the company Quality Management System by the Notified Body, together with the review of the required Technical Documentation, is a major element which the Notified Body takes into account to issue the certificate of conformity to the company product(s). Although the European Union Directives do not mandate certification to ISO 9001 and/or ISO 13485 the preferred method to prove compliance to such standards is to seek its official certification which is issued by certifying organizations known as 'Registrars'. One of the major requirements to prove conformity is the implementation of the Quality Management System according ISO 9001 and/or ISO 13485 and ISO 14971. The conformity of Medical Devices and In-vitro Diagnostic Medical Device according to European Union Directives 93/42/EEC, 90/385/EEC and 98/79/EEC must be assessed before sale is permitted.

specific requirements for cleanliness of productsД¬ompliance with ISO 13485 is often seen as the first step in achieving compliance with European regulatory requirements.

#WHAT IS THE DIFFERENCE BETWEEN ISO 13485 AND 21 CFR 820? VERIFICATION#

specific requirements for verification of the effectiveness of corrective and preventive actions.specific requirements for documentation and validation of processes for sterile medical devices.specific requirements for inspection and traceability for implantable devices.focus on risk management activities and design control activities during product development.

controls in the work environment to ensure product safety.Food and Drug Administration (FDA), or the Medical Devices Directive 93/42/EEC, required for doing business in the European Union Examples of market-specific regulatory requirements include 21 CFR 820, the Quality System Regulation for medical devices sold in the United States, enforced by the U.S. the promotion and awareness of regulatory requirements as a management responsibility.Additionally, the ISO 9001 requirements regarding customer satisfaction are absent from the medical device standard. A principal difference, however, is that ISO 9001 requires the organization to demonstrate continual improvement, whereas ISO 13485 requires only that the certified organization demonstrate the quality system is effectively implemented and maintained. While it remains a stand-alone document, ISO 13485 is generally harmonized with ISO 9001. Though it is tailored to the industry's quality system expectations and regulatory requirements, an organization does not need to be actively manufacturing medical devices or their components to seek certification to this standard, in contrast to the automotive sector's ISO/TS 16949, where only firms with an active request for quotation, or on the bid list, of an International Automotive Task Force supply chain manufacturer can seek registration.

What is the difference between iso 13485 and 21 cfr 820?