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Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions requirements in a cGMP environment are often overlooked as a Company develops new products. Depending upon the product being developed, e.g., tablets and capsules vs. biotechnology products to include recombinant microorganisms and gene therapy products, as few as fifteen to twenty or as many as sixty raw materials need to be sourced before the process can be moved from initiation through completion.
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Timings09:00 AM-06:00 PM (expected)Not Verified | Entry FeesPaid Ticket Check Official Website |
Estimated Turnout100 - 500 Delegates Based on previous editions | Event TypeConference |
EditionsApr 2020+5 more editions Frequency Biennial | Official LinksWebsiteContactsReport Error Claim this event |
Different Located Editions Philadelphia, USA27 - 28 Mar 2023 Boston, USA04 - 05 Nov 2021 3 Followers Orlando, USA04 - 05 Nov 2021 1 Followers San Diego, USA03 - 04 Oct 2019 1 Followers | |
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