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发表于 2015-6-21 22:45:18
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Part 3
Nature of non-compliance : The company was not operating its aseptic manufacture operations in compliance with EU GMP Annex 1. This was evident from by the high number of observations regarding the aseptic manufacturing facilities design, equipment, operations, environment monitoring and media fill validation. However, the QA system of the company failed to notice these problems and therefore was considered weak and inappropriately implemented. Detailed list of critical and major deficiencies is included in regulatory risk assessment
Action taken/proposed by the NCA :
Withdrawal, of current valid GMP certificate No. 004/2012/RO
current GMP certificate will be reissued to include only non-sterile products. A restricted GMP Certificate will be issued for sterile critical medicinal products for Romania, France, and UK
Requested Variation of the marketing authorisation(s)
change of API supplier
Prohibition of supply
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Suspension or voiding of CEP (action to be taken by EDQM)
suspension of CEPs
请问restricted GMP certificate是指什么意思??? |
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