Keyword: manufacturer

Product Matches
Name Summary SKU
GOST R 55747-2013 Guidelines for regulatory auditing of quality management systems of medical device manufacturers. Part 5. Audits of manufacturer control of suppliers RUSS64696
GOST R IEC 62304-2013 Medical device software. Software life cycle processes RUSS74105
GOST R 55544-2013 Medical devices software. Part 1. Guidance on the application of ISO 14971 medical devices software RUSS74127
GOST R IEC 62366-2013 Medical devices. Application of usability engineering to medical devices RUSS74289
GOST EN 848-2-2013 Safety of woodworking machines. One side milling machines. Part 2. Single spindle milling machines with vertical upper arrangement of spindle RUSS43916
GOST R 51849-2001 Compound feed production. Information for consumer. General requirements RUSS66164
PR 50-718-99 Requirements for Compiling and Submitting Product Data Sheets RUSS149349
GOST R ISO 15198-2009 Clinical laboratory medicine. In vitro diagnostic medical devices. Validation of user control procedures by the manufacturer RUSS60840
GOST R 54882-2011 Guidelines for regulatory auditing of quality management systems of medical device manufacturers. Part 2. Regulatory auditing strategy RUSS70818
GOST R 55754-2013 Complex quality control system. Electronic components. System of relationship between manufacturers and customers RUSS70867
GOST R 51725.12-2014 Catalogization of products for federal state needs. The registration order for researchers, manufacturers and suppliers of products for federal state needs RUSS287541
GOST R 55251-2012 Air transport. Automatic control of technical condition of aircraft products. Information and analytical system for aircraft airworthiness monitoring. The «Manufacturer» user module. General requirements RUSS59753
GOST R 50995.0.1-96 Technological supplement for products development and production. Basic principles RUSS60381
GOST R 54421-2011 Guidelines for regulatory auditing of quality management systems of medical device manufacturers. Part 1. General requirements RUSS69708
GOST R 54881-2011 Guidelines for auditing of quality management systems of medical device manufacturers to conform to regulating requirements. Part 3. Audit report RUSS61754
GOST EN 13795-1-2011 Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment. Part 1. General requirements RUSS62788
GOST R 55748-2013 Guidelines for regulatory auditing of quality management systems of medical device manufacturers. Part 4. Multiple site auditing RUSS71035
GOST R IEC 62911-2018 Audio, video and information technology equipment. Routine electrical safety testing in production RUSS354341
GOST R 59765-2021 Software as a medical product. Basic terms and definitions. RUSS428357
GOST R 51087-97 Tobacco products. Information for consumer RUSS62869
GOST R EN 13795-1-2008 Surgical drapes, gowns and clean air suits used as medical devices, for patients, clinical staff and equipment. Part 1. General requirements RUSS63209
GOST R ISO 15621-2012 Urine-absorbing aids. General guidelines on evaluation RUSS63241
GOST R IEC 60601-1-6-2014 Medical electrical equipment. Part 1-6. General requirements for basic safety and essential performance. Collateral standard. Usability RUSS72332
GOST 32562.4-2013 Coatedglass. Acceptance rules RUSS72806
GOST R IEC 62075-2011 Audio/video, information and communication technology equipment. Environmentally conscious design RUSS72834
ODM 218.3.112-2019 Guidelines for the development and approval of technological regulations for production at the enterprises of the road sector RUSS374250
GOST R 56018-2014 Instructions for use of products by consumers RUSS44218
 

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