EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use

@inproceedings{January2009EUGT,
  title={EU Guidelines to Good Manufacturing Practice Medicinal Products for Human and Veterinary Use},
  author={January},
  year={2009}
}
  • January
  • Published 2009
  • Medicine
  • This guidance applies to capping operations performed as an aseptic process using sterilized caps or as a “clean process” that is performed outside the aseptic core using clean non-sterilized caps. It is important to note that there may be other additional regional/local area requirements or expectations for capping operations that supersedes the information specified within EU GMP Annex 1 that must be considered (e.g. Irish Medicines Board (IMB) or the Medicines and Healthcare Products… CONTINUE READING
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