Sterile Manufacturing – Qvents

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Updated on October 11, 2023

Updated on October 11, 2023

USFDA : Sterile Drug Products Produced by Aseptic Processing — Current Good Manufacturing Practice – Guidance
USFDA : Submission Documentation for Sterilization Process Validation in Applications for Human and Veterinary Drug Products – Guidance
USFDA : Sterilization Process Controls (Inspection)
USP 1211: Sterilization And Sterility Assurance Of Compendial Articles (Access and read USP Chapter 1211))
Europe: Annexure 1, Manufacture of Sterile Medicinal Products (EudraLex – Volume 4 – Good Manufacturing Practice (GMP) guidelines)
EMA : Sterilisation of the medicinal product, active substance, excipient and primary container – Scientific guideline
PICS: Revised Annex 1 (Manufacture of Sterile Medicinal Products) /Guide to Good Manufacturing Practice for Medicinal products
PICS::Validation of Aseptic Processes (Jan 2011)
WHO: TRS 1044 – Annex 2: WHO good manufacturing practices for sterile pharmaceutical products (WHO Technical Report Series, No. 1044, 2022)
WHO: Good Manufacturing Practices For Sterile Pharmaceutical Products (WHO Technical Report Series, No. 961, 2011)
ISPE : Validation of Aseptic Processes Using Media Fill
PDA Technical Report No. 22 (Revised 2011): Process Simulation for Aseptically Filled Products
PDA Technical Report No. 28 Revised, (TR 28) Process Simulation Testing for Sterile Bulk Pharmaceutical Chemicals (single user digital version)
ISO 13408-1:2008 : Aseptic processing of health care products (Access to the documented is a paid service)

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