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Particle Measuring Systems (PMS) Training
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EU GMP Annex 1 Revision 2017 Draft - Webinar
On December 20th, 2017, the draft for a Revision of ANNEX 1 (“Manufacture of Sterile Medicinal Products”) of the EU Guideline for GOOD MANUFACTURING PRACTICE for drug products and drug substances was published. This updated guidline will set a milestone for adjustments needed within European agencies overseeing drug products regulatory applications. During the creation process, the US FDA and PIC/S were consulted by and partnered with the EU ...