Pharmaceutical Microbiology Manual
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ORA.007 Pharmaceutical Microbiology Manual
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- Revised: 25 Aug 2020 Title: Pharmaceutical Microbiology Manual
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OOD AND D RUG A DMINISTRATION O FFICE OF R EGULATORY A FFAIRS Office of Regulatory Science Document Number: ORA.007 Revision #: 02 Revised: 25 Aug 2020 Title: Pharmaceutical Microbiology Manual Page 83 of 92 For the most current and official copy, check QMiS. d. CFR 820 “Quality Systems Regulation (Devices, not covered) e. CFR 314.81(b)(3)(ii)- Applications for FDA approval to market a new drug (revised April 1, 2008) For submission of an alternate microbiological method with a comparability study f. CFR 1271 Human cells, tissues, and cellular and tissue-based products 2. FDA Compliance Program Guidance Manuals a. FDA Compliance program Guidance Manual for FDA Staff: Drug Manufacturing Inspections program 7356.002 During an inspection this program designated six (6) critical systems for review. They include: Quality System (always covered during an FDA inspection); Facilities &Equipment; Material; Production; Packaging and labeling; and Laboratory control systems. b. FDA Compliance program Guidance Manual for FDA Staff: Sterile Drug Process Inspections 7356.002A The sections entitled “Inspectional” and “Analytical” and “Attachment A” are pertinent to an FDA microbiologist. 3. Compliance Policy Guides a. Sec. 100.550- Status and Responsibilities of Contract Sterilizers Engaged in the Sterilization of Drugs and Devices (CPG 7150.16) (Oct 2006) b. Sec. 490.100 Process Validation Requirements for Drug Products and Active Pharmaceutical Ingredients Subject to Pre-Market Approval (CPG 7132c.08) (3/2004) c. Manual of Policies and Procedures, CDER, MAPP 5040.1 Product Quality Microbiology Information in the Common Technical Document - Quality (CTD- Q) d. Compliance Policy Guidance for FDA Staff- Sec. 280.110 Microbiological Control Requirements in Licensed Anti-Human Globulin and Blood Grouping Reagents 4. US Pharmacopeia (USP) Compendium Review all relevant product monographs (not all have microbiological requirements); the following are regulatory chapters that contain enforceable microbiology requirements General Notices and Requirements (page 1-13), Chart 10- Microbiology |
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