Free Live Webinars for Pharma Professionals

Our pharma webinars cover GMP, process validation, equipment qualification, data integrity, CAPA, inspection readiness, CSV, lab compliance and regulatory updates for the pharmaceutical and biotech sectors.

Most of our pharma webinars are free live events, sponsored by industry partners; on‑demand recordings and private virtual classes may have fees.

Webinars provide training, practical templates and expert guidance that improve inspection readiness, reduce deviations, and strengthen quality systems.

Most pharma webinars run 45–90 minutes, including a 15–30 minute live Q&A. Recorded sessions often include the full presentation and downloadable slide packs.

All of our pharma webinars provide a certificate of attendance. A selection of courses and virtual classes offer continuing education (CE) credits — check the webinar details for accreditation information.

Yes. While content targets pharma, biotech and medtech professionals, suppliers, CROs, consultants and auditors can also benefit from sessions on GMP, validation and regulatory compliance.

 Webinars on documentation control, CAPA, deviation management, supplier qualification and inspection preparation provide practical checklists, mock-audit tips and corrective action strategies to strengthen audit readiness.

Yes. We offer sponsorship and partnership packages for co-branded pharma webinars and events. Contact our partnerships team for options and guidelines.

Yes. We regularly cover FDA, EMA and other regulators’ guidance, inspection trends and enforcement updates as they relate to GMP, data integrity, validation and quality systems.

Yes. Live webinars include moderated Q&A and polls. Speakers often provide follow-up resources and may answer selected attendee questions after the session.