Recent Episodes
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Crystal Ball Gazing: What Does the Future Hold for Regulatory Affairs in Drug Development for 2025
Mar 17, 2025 – 32:57 -
How to Effectively De-Risk your IND Process
Feb 11, 2025 – 52:58 -
Understanding EU Medical Device Regulations: Key Insights for Developers and Innovators
Jan 7, 2025 – 24:03 -
Patients as Partners: Advocacy's Role in Shaping Drug Development
Nov 8, 2024 – 27:24 -
Navigating the Future of EU Health Technology Assessments
Oct 16, 2024 – 29:10 -
A Guide to Marketing Authorization Applications in Europe
Sep 24, 2024 – 28:19 -
Navigating the new EU Clinical Trials Regulation
Aug 13, 2024 – 28:26 -
Advances in Cell-Based Immunotherapies: CAR-T Cell Therapy vs TCR Therapy
Jul 25, 2024 – 28:10 -
Demystifying Regulatory Designations in Drug Development
Jul 10, 2024 – 25:53 -
Exploring Genome Editing Technologies in Drug Development
Jun 19, 2024 – 23:44 -
The Most Essential Tips for Biotechs Seeking Investment
Jun 3, 2024 – 23:17 -
The Use of ATMPs in Oncology Clinical Trials
May 21, 2024 – 19:54 -
How are GMO Regulations Impacting Clinical Development in Europe?
Apr 25, 2024 – 24:53 -
US Drug Development: The Latest Regulatory Trends and Initiatives
Mar 19, 2024 – 22:38 -
The Regulatory Challenges of Rare Disease Drug Development
Feb 28, 2024 – 29:37 -
The Drug Development Landscape: Trends and Predictions for 2024
Jan 22, 2024 – 25:40 -
Off-the-Shelf Cell Therapies: Breaking Barriers and Revolutionizing Patient Care
Dec 4, 2023 – 20:30 -
The Future of Drug Development: AI’s Role in Revolutionizing the Industry
Nov 8, 2023 – 22:13 -
Recent Trends in Oncology Drug Development
Oct 4, 2023 – 25:14
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