Description
From Molecule to Market: R&D And Regulatory Considerations builds on the business overview of the Intro to Business course. This course delivers an outline of clinical, regulatory, and quality considerations and practices. Attendees will be provided foundational information about the Biopharma industry and regulations via instruction, storytelling, and breakout group discussions. Applied industry ethics will be discussed with emphasis on historical precedents. The course will explore the decision-making process by touching on relevant topics such as market share and phases of development.
Schedule
- Monday, May 15th, 2023, 10:00 AM – 12:30 PM EST
- Tuesday, May 16th, 2023, 10:00 AM – 12:30 PM EST
- Thursday, May 18th, 2023, 10:00 PM – 12:30 PM EST
Agenda
Session 1:
- The History of Regulations
- Industry Overview
- Research & Development: An Overview of R&D
Session 2:
- Roles in Clinical Trials
- Marketing Considerations
Session 3:
- Compliance via Regulatory & Quality Processes