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Fda Cfr

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1 Fda.com Information Portal
On-Line Discussion Groups and Information Portal serving the Pharmaceutical, Biotechnolgy, Medical Device, Food and Cosmetic Regulated Industry by Industry Professionals. FDA.COM is the next step for professionals seeking compliance information through discussion groups and on-line information sharing. Directed by John Cuspilich, Director ...

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2 Welcome To Gmp Publications
Code of Federal Regulations Mini-Handbooks as provided by the Food and Drug Administration FDA. The laws for Pharmaceuticals, BioTechnology, Medical Device and Regulatory Industry. Quality Assurance QA, Blood, Biologics, Drug and Food Industry

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3 Cfr - Code Of Federal Regulations Title 21
The information on this page is current as of April 1 2018. For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR).

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4 Compliance Actions And Activities
This page provides links, for example, to documents, lists, policies, programs, and statements relating to Compliance References used by FDA personnel:

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5 Cfr - Code Of Federal Regulations Title 21
This information is current as of April 1, 2018. This online reference for CFR Title 21 is updated once a year. For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR).

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6 Fda 21 Cfr Part 11 - Mastercontrol Inc
MasterControl's FDA 21 CFR Part 11 Compliant Quality System. MasterControl has developed state-of-the-art document control and quality management solutions that are 100% compliant with FDA 21 CFR Part 11 regulations.

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7 Part 11, Electronic Records; Electronic Signatures …
II. BACKGROUND. In March of 1997, FDA issued final part 11 regulations that provide criteria for acceptance by FDA, under certain circumstances, of electronic records, electronic signatures, and ...

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8 Fda Glp Compliance | 21 Cfr Part 58 | Qa …
QA Consulting and Testing, LLC is the industry leader in 21 CFR Part 58 of FDA Good Laboratory Practice for non-clinical laboratory studies. We have been assisting companies like yours with 21 CFR Part 58 needs for over a decade.

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