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Product image for Good Manufacturing Practices (cGMP) 12 hrs Training Online

Good Manufacturing Practices (cGMP) 12 hrs Training Online

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.

Course•By Kelly Thomas

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Product image for Regulatory Compliance for Dietary Supplements in the US, EU and Canada

Regulatory Compliance for Dietary Supplements in the US, EU and Canada

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

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Product image for REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance

19-20 Aug This 2 day seminar will go into the specifics of the REACH and RoHS regulations

Course•By Kelly Eisenhardt

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Product image for Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products 2 Day Course

Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products 2 Day Course

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

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Product image for Technical Writing 20 Hours Course for Medical Devices, Pharma and Biotech

Technical Writing 20 Hours Course for Medical Devices, Pharma and Biotech

MP3 Download Online Technical Writing Course for pharmaceutical, biotech, and medical device professionals.

Course•By Charles H. Paul

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Product image for FDA Inspection Readiness in the AI Era 2026

FDA Inspection Readiness in the AI Era 2026

MP3 Download Understand how FDA AI-driven targeting may impact inspections

Course•By Kelly Thomas

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Product image for Advanced Pharmacovigilance Auditing and Inspections Virtual Live Training Course

Advanced Pharmacovigilance Auditing and Inspections Virtual Live Training Course

MP3 Download Pharmacovigilance Auditing Inspection course will explain how to prepare for the audit

Course•By Michael Ramcharan

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Product image for The EU Clinical Trial Regulation - EU Filings & Registrations 6 hrs Course Online

The EU Clinical Trial Regulation - EU Filings & Registrations 6 hrs Course Online

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

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Product image for Statistical Process Control (SPC) Training

Statistical Process Control (SPC) Training

MP3 Download This seminar will provide attendees with the statistical tools necessary to monitor processes to ensure the quality

Course•By Elaine Eisenbeisz

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Product image for Biostatistics for the Non-Statistician

Biostatistics for the Non-Statistician

MP3 Download this course will have understanding of concepts and statistical methods required in pharmaceutical, biological and medical device.

Course•By Elaine Eisenbeisz

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Product image for Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Product

Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Product

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

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Product image for 21 CFR Part 11 Compliance for SaaS/Cloud Application

21 CFR Part 11 Compliance for SaaS/Cloud Application

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

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Product image for Risk-based Computer System Validation; Reduce Costs and Avoid 483s

Risk-based Computer System Validation; Reduce Costs and Avoid 483s

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

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Product image for Project Management for Non-Project Managers – PM in the Life Sciences – Pharmaceutical/ Biotechnology and Medical Devices

Project Management for Non-Project Managers – PM in the Life Sciences – Pharmaceutical/ Biotechnology and Medical Devices

MP3 Download This virtual seminar will address those project management critical tasks within each project phase that must be performed

Course•By Charles H. Paul

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Product image for Computer System Validation for Cloud and COTS Applications–Live, Online Training

Computer System Validation for Cloud and COTS Applications–Live, Online Training

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

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Product image for All About Data Integrity by Design

All About Data Integrity by Design

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

Course•By Carolyn Troiano

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Product image for Navigating the Medical Device Post-Market Maze and Challenges during COVID-19 Pandemic - Learn what FDA is really thinking on regulation and guidance documents

Navigating the Medical Device Post-Market Maze and Challenges during COVID-19 Pandemic - Learn what FDA is really thinking on regulation and guidance documents

MP3 Download this course will explain how to comply with complicated Complaint Handling, MDR and Recall requirements. Earl Bird. Register.

Course•By Kelly Thomas

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Product image for EU MDR Implementation and Transitioning to the Deadline: Essential Tasks to Complete

EU MDR Implementation and Transitioning to the Deadline: Essential Tasks to Complete

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

Course•By Kelly Thomas

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Product image for 2 Day Virtual Seminar on FDA Inspection Essentials in 2022

2 Day Virtual Seminar on FDA Inspection Essentials in 2022

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

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Product image for Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines

Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines

MP3 Download This 2-day seminar will explain the new Analytical Procedure Lifecycle guidelines and give attendees the knowledge needed to implement recommend

Course•By Kelly Thomas

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Product image for FDA QMSR Transition and New FDA Inspection Requirements Replacing QSIT Course

FDA QMSR Transition and New FDA Inspection Requirements Replacing QSIT Course

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

Course•By John E Lincoln

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