Current Regulatory Requirements for Aseptically Produced Products
January 17, 2019 - Online Event ON CAWebinar Compliance
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The manufacture of sterile products, whether by aseptic means or terminal sterilization, requires a thorough understanding of applicable regulations by the FDA and those by the EU if selling your products overseas. In addition, there are various guidance documents that address other issues such as closure integrity and sterility test methods that were recently revised.
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