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Jul 20-23, 2026, Time 12:00 PM – 05:00 PM EST Online Technical Writing Course for pharmaceutical, biotech, and medical device professionals.
Course•By Charles H. Paul
July 22-23 Pharmacovigilance Auditing Inspection course will explain how to prepare for the audit
Course•By Michael Ramcharan
July 22-23, 2026, Time 12:30pm-5:00pm EST Understand how FDA AI-driven targeting may impact inspections
Course•By Kelly Thomas
Jul 27-30 - Time 12:00 PM – 05:00 PM ET Master the fundamentals of Good Manufacturing Practices (cGMP) in this engaging 4 half-day virtual training designed for pharmaceutical, biotech, and laboratory professionals, aligned with regulations from the U.S. Food and Drug Administration.
Aug 12-13 This 2-day interactive virtual seminar will review the regulations that impact Dietary Supplements in the US, EU and Canada
Course•By Travis Austin MacKay
19-20 Aug This 2 day seminar will go into the specifics of the REACH and RoHS regulations
Course•By Kelly Eisenhardt
Aug 24-25 The objective of this live, interactive WCS training seminar is to explore the role of aseptic filling to assure that manufactured product
Course•By Barry A. Friedman
MP3 Download Gain a comprehensive and practical understanding of EU Clinical Trial Regulation (EU CTR 536/2014) and learn how to manage filings, submissions, and regulatory processes effectively across the European Union.
Course•By John E Lincoln
MP3 Download This seminar will provide attendees with the statistical tools necessary to monitor processes to ensure the quality
Course•By Elaine Eisenbeisz
MP3 Download this course will have understanding of concepts and statistical methods required in pharmaceutical, biological and medical device.
MP3 Download In this course, you will learn the practical applications for ensuring regulatory compliance as required by FDA regulations
Course•By Karl M. Nobert
MP3 Download This course benefits anyone that uses computer systems to perform their job functions and is ideal for professionals working in the health care, clinical trial, biopharmaceutical, and medical device sectors
Course•By David Nettleton
This course benefits anyone that uses computer systems to perform their job functions and is ideal for professionals working in the health care, clinical trial, biopharmaceutical, and medical device sectors
MP3 Download This virtual seminar will address those project management critical tasks within each project phase that must be performed
MP3 Download The attendee will learn about FDA’s approach to modernizing technology, and how that will benefit both the Agency and industry
Course•By Carolyn Troiano
MP3 Download The course provides insight into the ways in which Pharma 4.0™ will serve as an enabler for next generation medicinal products and new business cases for established products
MP3 Download this course will explain how to comply with complicated Complaint Handling, MDR and Recall requirements. Earl Bird. Register.
MP3 Download This 2-day virtual seminar will go into the specifics of the European Union Medical Device Regulation (EU MDR), provide case studies and share le
MP3 Download This seminar, you will learn how to properly alert key members that an investigator has arrived, the proper protocol
Course•By Danielle DeLucy
MP3 Download This 2-day seminar will explain the new Analytical Procedure Lifecycle guidelines and give attendees the knowledge needed to implement recommend
June 17th, 2026 at 11:00 AM - 02:00 PM EST Understand FDA’s New QMSR Inspection Model, ISO 13485 Alignment, and What Replacing QSIT Means for Medical Device Compliance in 2026
