Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
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Deadline: July 06, 2020 | Date: July 16, 2020-July 17, 2020
Venue/Country: Virtual Seminar, U.S.A
Updated: 2020-05-13 22:59:35 (GMT+9)
Call For Papers - CFP
Raw material 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.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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