Houston LNG Virtual Event: Regulatory Affairs and the Law Profession with Julie Tierney

Regulatory affairs sit at the intersection of science, policy, and law—shaping how pharmaceutical and biotechnology innovations move from the laboratory to the market. This educational webinar explores the evolving regulatory landscape governing the pharmaceutical and biotech industries, with a particular focus on the critical role of legal professionals in navigating compliance, risk, and strategy.

Designed for attorneys, regulatory affairs professionals, compliance officers, scientists, and students interested in life sciences law, the session will provide a practical overview of how regulatory frameworks impact product development, clinical trials, manufacturing, and commercialization. Attendees will gain insight into key regulatory bodies, approval pathways, and enforcement mechanisms, as well as emerging trends that are redefining regulatory practice in a rapidly advancing scientific environment.

The webinar will also examine how the law profession supports innovation while safeguarding public health, highlighting collaboration between legal teams, regulatory experts, and scientific stakeholders. Topics will include regulatory strategy, compliance challenges, ethical considerations, and the increasing complexity of global regulatory harmonization.

Through expert discussion and real-world examples, this session aims to demystify regulatory affairs and clarify how legal expertise adds value across the pharmaceutical and biotech lifecycle. Whether you are seeking foundational knowledge or looking to deepen your understanding of regulatory law in the life sciences, this webinar offers timely insights into one of the most influential—and dynamic—areas of modern legal and regulatory practice.

Registration Fees & Deadlines

Free

Proof of Attendance

A certificate of attendance can be downloaded from the RAPS Learning Portal following the event.

Questions