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on
1
Intro
2
Challenges in CMC
3
Kick Off Meeting
4
CMC acronyms
5
Drug companies
6
Phase 3 trials
7
Drug requirements
8
Evan Hecker
9
Dr John OBrien
10
CMC Process
11
Technical Stagegate Deliverables
12
GMP Starting Material
13
Supplying the Clinic
14
Raw Materials
15
Supply the Clinic
16
Supporting Clinical Development
17
Validation
18
Commercial
19
Volumetric Efficiency
20
Registration Material
21
Points to Consider
22
Planning
23
Timeline
24
Changing the Product
25
Regulatory CMC
26
Bridge the Clinical Program
27
Registration Stability Program
Description:
Explore the intricate journey of transforming a molecule into a physical medicine for human use in this comprehensive 1 hour 49 minute workshop from the American Society for Microbiology's Antibiotic Development Bootcamp. Delve into the critical aspects of Chemistry, Manufacturing, and Controls (CMC) with expert discussants from Spero Therapeutics, Tedor Pharma Inc, and Syner-G Pharma Consulting. Learn about the challenges in CMC, technical stage-gate deliverables, GMP starting materials, clinical supply processes, and regulatory considerations. Gain insights into the complexities of drug development, from raw materials to commercial production, including validation, volumetric efficiency, and registration stability programs. Understand the importance of planning, timelines, and potential product changes throughout the development process. This workshop, part of the 2017 ASM/ESCMID Conference on Drug Development to Meet the Challenge of Antimicrobial Resistance, offers valuable knowledge for professionals in the pharmaceutical and microbiology fields. Read more

Antibiotic Bootcamp - How Does a Molecule Become a Physical Medicine to be Given to a Human

American Society for Microbiology
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