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关于文件保存期限的请教,谢谢
大家好,
我们近期在整理、销毁记录,对文件记录的保存期多少还是有些纠结,特别是辅助记录,如货位卡、设备日志、内审报告等,请问大家都是按什么周期保存的,谢谢
查了How to do文件:6.1 Documentation System and Specification
6.12
It is good industry practice to consider retaining records for the period of time the drug product(s) in which the API was used may be available on the market.
Examples for minimum retention periods of supporting documents are:
- clinical batches for an IND or NDA (see also chapter 19) LC + 1 year
- batches for bioequivalence testing LC + 1 year
- product development reports LC + 1 year
- development and validation reports of analytical test procedures LC + 1 year
- process validation reports LC + 1 year
- equipment IQ, OQ and PQ reports LC + 1 year
- supporting systems (e.g. utilities, computerised systems) LC + 1 year
- training records indefinitely
(for clinical trials and demonstration batches LC + 1 year should be considered)
Note: LC means “life cycle” of the product where shelf life is included. “Life cycle” means the process starting with the user requirements, continues through design, real-isation, qualification, process validation and maintenance until the stadium “status” of not in use.
Electronic data should comply to the same record retention principles.
Electronic data should follow the applicable regulations such as Eudralex Vol 4, An-nex 11: Computerised Systems for the EU.
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