2020 - Essentials Of USP Microbiology - Reading Between the Lines of the USP General and Information Microbiology Chapters
Date2020-06-25 - 2020-06-26
Deadline2020-09-06
VenueChicago, IL, USA - United States
KeywordsDrug development process; Identification of drug targets; Pharmacokinetics
Topics/Call fo Papers
This course is designed to cater for employees of pharmaceutical companies who would like an understanding of the drug development and regulatory approval process. The course starts by considering the global pharmaceutical market, important therapeutic areas and the roles of different pharmaceutical professionals in the development process, as well as a definition of drugs and medical devices. The drug development process, from discovery to post-marketing surveillance, is then explained. Topics include the identification of drug targets, synthesis of chemical drugs and the development of biologics, pharmacokinetics and toxicity screening, pre-clinical development, clinical studies, regulatory submissions, managing post-approval change, pharmacovigilance and an overview of regulations governing drug manufacture and distribution.
Other CFPs
- Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
- Technical Writing for Pharma, Biotech and Med Devices
- Pharmaceutical Dissolution Testing
- HIPAA Security and Breach Rule Compliance- Understanding Risk Analysis, Policies and Procedures and Managing Incidents
- HIPAA Security and Breach Rule Compliance- Understanding Risk Analysis, Policies and Procedures and Managing Incidents
Last modified: 2020-01-14 00:56:12