PDA TR 77

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PDA TR 77

2017

Most Recent

Technical Report No. 77 (TR 77) The Manufacture of Sterile Pharmaceutical Products Using Blow-Fill-Seal Technology

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PDA's newly released Technical Report No. 77 (TR 77), The Manufacture of Sterile Pharmaceutical Products Using Blow-Fill-Seal Technology provides recommendations specific to the operation of blow-fill-seal (BFS) technology for the manufacture of sterile pharmaceuticals (e.g., ophthalmic, parenteral, and inhalation). The intent of this document is to provide supplemental information to assist the user with interpretation of international standards and regulatory guidance from the perspective of BFS operations. Consideration is given to specific aspects of BFS operations not covered in published information. This Technical Report addresses considerations for BFS technology related to the installation and operation of machinery and evaluation of related materials and final product containers. Support areas such as laboratory, solution compounding, gowning airlocks, etc. are not considered specific to blow-fill-seal and are not included within the scope of this document. This technical report is intended as a guide for the industry and is not meant to supplant or duplicate any existing regulatory guidance.

PDA TR 77
STANDARD INFO:
Standard NamePDA TR 77
ScopeTechnical Report No. 77 (TR 77) The Manufacture of Sterile Pharmaceutical Products Using Blow-Fill-Seal Technology
PublisherPDA - Parenteral Drug Association
LanguagesEnglish
State
Publication Year2017
Most recent VersionMOST RECENT
Whether to be replaced
Addendum
FILE INFO:
File Size1 file , 830 KB
ISBN(s)9780939459940
Number of Pages40
Product Code(s)01077
Published02/01/2017
PDA TR 77
HistoryPublisher Year

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