This group focuses on the scientific, quality and regulatory aspects of pharmaceutical, biotech, ATMP and regulated healthcare manufacturing. Relevant topics of discussion may include quality and testing initiatives in support of production and product release, GMPs and compliance, updates to pharmacopoeia chapters and drug regulations, and associated guidances. The moderators review all requests to join the group; If you were not approved, please DM the Group Owner. Posts which are outside the scope of the group (as described above) will be rejected without notice. We also reject posts that self-promote yourself or your company's products or services (except on our quarterly supplier days). We encourage announcements for relevant technical conferences, training programs, publications and employment opportunities that are aligned with the scope of this group. PLEASE READ THE FULL GROUP RULES BEFORE SUBMITTING POSTS.