Live Regulatory Training

Expert-Led Live Sessions for Pharmaceutical, Medical Device, Biotech and Life Sciences Professionals. Delivered on Fixed Dates. 
Explore the current schedule below for upcoming live sessions across the regulatory and compliance areas covered by TalkFDA. New programs are added regularly as regulatory requirements and industry priorities evolve.

Upcoming Live Webinars

Each session is conducted live on the scheduled date. Registration closes prior to the event.

Prefer Continuous Access?

For ongoing access to expert-led programs beyond scheduled sessions, explore TalkFDA subscription options.

Live Training Across Key Regulatory & Compliance Areas

TalkFDA's live training schedule changes regularly, but the subject areas remain focused on the regulatory, quality and compliance needs of regulated life sciences organizations. Upcoming programs may cover:

FDA & US Regulatory Training

FDA Regulations, Regulatory Affairs, Regulatory Strategy, FDA Meetings, Inspections, Submissions And Compliance Expectations.

EU & Global Regulatory Training

EU MDR, EMA, MHRA, ICH and other international regulatory requirements.


Pharmaceutical & GMP Training

GMP requirements, pharmaceutical quality systems, manufacturing compliance, investigations, CAPA, validation and process monitoring.

Medical Device Regulatory Training

EU MDR, FDA medical device requirements, medical device compliance, QMSR, 510(k), design controls, validation and regulatory submissions.


Quality, Validation & Data Integrity Training

Quality systems, quality assurance, computer system validation (CSV), Computer Software Assurance, process validation, equipment qualification, electronic records and data integrity.

Clinical, GCP & GxP Training

Good Clinical Practice (GCP), clinical research, clinical trial requirements, TMF/eTMF and broader GxP requirements.


TalkFDA Elite Training Labs TM

Private workshop delivery structured for internal deployment.