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From Molecule to Market: R&D and Regulatory Considerations
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.
Session 1: Monday, May 9th, 2022 12:00-2:30 PM EST
The History of Regulations
Research & Development: An Overview of R&D
Session 2: Wednesday, May 11th, 2021 12:00-2:30 PM EST
Roles in Clinical Trials
Session 3: Thursday, May 12th, 2021 12:00-2:30 PM EST
Compliance via Regulatory & Quality Processes
Please view the discount options for courses before registering here.
If you are registered for Intro to Biotech or have taken the course in the past year, you are eligible to receive a 10% discount applied to your registration of From Molecule to Market: R&D and Regulatory Considerations. Contact firstname.lastname@example.org to obtain the coupon code to enter when checking out.
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