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Medical device Training (104)
FDA Regulatory Compliance Training (302)
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Biotechnology Online Courses and Training (236)
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Healthcare Training (13)
Virtual Seminars (83)
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Europe Seminars (32)
USA Seminars (48)
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Alan Golden
Amanda McFarland
Andrew Campbell
Angela Bazigos
Barry A. Friedman
Ben Marandi
Carl Patterson
Carolyn Troiano
Casper (Cap) Uldriks
Charity Ogunsanya
Charles H. Paul
Cynthia Brysch
Danielle DeLucy
David Jones
David L. Chesney
David Nettleton
David R. Dills
David W. Husman
Dr. Afsaneh Motamed Khorasani
Dr. John M. Ryans
Dr. Michael Abitz
Dr. Stefano Persiani
Edwin Waldbusser
Elaine Eisenbeisz
Frank Stein
Ginette Collazo
Graeme Ladds
Jan Seal
Jeff Kasoff
Jim Sheldon-Dean
Joanna Brougher
John C. Fetzer
John E Lincoln
John G. Lanese
Jose Mora
Jose Mora
Joy L. McElroy
Karl M. Nobert
Kelly Eisenhardt
Kelly Thomas
Lisa Hardwick Thompson
Mark Brengelman
Mark Hughes
Mark Powell
Martin K. Behr
Meena Chettiar
Michael Esposito
Michael Ramcharan
Nancy Knettell
Nissan Cohen
Paolo Giacomoni
Paul Larocque
Peggy J. Berry
Peter Reijntjes
Rita Hoffman
Rob MacCuspie
Roger Cowan
Ron Snee
Speaker
Speaker for Biotechnology
Steven Laurenz
Susanne Manz
Theodore Sand
Tim Fischer
Todd Graham
Travis Austin MacKay
Trisha Paul
William Mack Copeland
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Fundamentals of Good Manufacturing Practices – Developing a Compliance Mindset
Available until
MP3 Download This webinar will discuss the basic principles and requirements for Good Manufacturing Practices
David W. Husman
%
COMPLETE
$199
Is My Data Abnormal? Normality Tests and Transformations Live Webinar
Available until
MP3 Download In this webinar, you will also learn tools and concepts to understand what makes a distribution normal and when a transformation of data
Elaine Eisenbeisz
%
COMPLETE
$299
Virtual Seminar on GAMP® Data Integrity 21 CFR Part 11 Training Course
Available until
MP3 Download This training course will provide a practical understanding of the requirement for a data governance framework
Carolyn Troiano
%
COMPLETE
$695
Webinar Analytical Method Validation and Transfer According to the New FDA Guidance
Available until
MP3 Download This course will prepare attendees with the knowledge and tools to plan and execute test method validation packages for the NDA
Kelly Thomas
%
COMPLETE
$499
QA and Risk Management approaches when Managing Clinical Trial Data – New Course !
Available until
MP3 Download This presentation focuses on the role of QA in the Risk Management process when deciding on how data should be collected
Carolyn Troiano
%
COMPLETE
$229
Post-Market Activities in the EU-MDR — A Detailed Analysis
Available until
MP3 Download Medical device training will review the new EU-MDR requirements governing Post Market Activities and discuss quality system approaches
Kelly Thomas
%
COMPLETE
$399
Are you ready for your next regulatory inspection? On site or virtual in 2021
Available until
MP3 Download This webinar is a practical, hands-on course designed to provide FDA industry with information and tools required to prepare for and manage an FDA
Alan Golden
%
COMPLETE
$399
Supplier Management: How to meet FDA QSR and ISO 13485 requirements in a cost effective manner
Available until
MP3 Download Duration 60 Minutes
Jeff Kasoff
%
COMPLETE
$179
Cosmetic Ingredients: from Science to Practical Use
Available until
MP3 Download Duration 90 Minutes
Paolo Giacomoni
%
COMPLETE
$199
Creating and Maintaining an Effective and Efficient Technical Training Program
Available until
MP3 Download Duration 180 Minutes
Ginette Collazo
%
COMPLETE
$299
Developing an Effective CAPA Management and Root Cause Analysis System
Available until
MP3 Download Duration 180 Minutes
Danielle DeLucy
%
COMPLETE
$499
The Healthcare Quality Improvement Act: Achieving Immunity in Your Peer Review Process
Available until
MP3 Download This webinar will discuss the Health Care Quality Improvement Act (HCQIA) in detail, including the standards that must be met to achieve immunity
William Mack Copeland
%
COMPLETE
$199
Continuing to Audit during a Global Pandemic – How to Optimize Effectiveness and Minimize Risk
Available until
MP3 Download Duration 60 Minutes
Susanne Manz
%
COMPLETE
$249
Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements
Available until
MP3 Download This webinar will give you a comprehensive understanding of this important subject with an emphasis on the different types of sterilizing
Roger Cowan
%
COMPLETE
$299
Knock, knock, who’s there? Are you ready for an FDA inspection in the COVID-19 Era and Beyond?
Available until
MP3 Download This webinar will help you manage inspections efficiently and effectively. You’ll learn about the FDA’s inspectional approach, focus areas
Susanne Manz
%
COMPLETE
$389
Sunscreens: Their Importance and US Regulations
Available until
MP3 Download Duration 90 Minutes
Paolo Giacomoni
%
COMPLETE
$199
Overview of Pharmacovigilance Under COVID-19
Available until
MP3 Download This Pharmaceutical training online aims to demonstrate what the new guidances allow in terms of pharmacovigilance activities that can be relaxed
Graeme Ladds
%
COMPLETE
$199
DHF, DMR, DHR, Technical Documentation for US FDA, ISO and EU MDR Requirements
Available until
MP3 Download / Online On Demand-Duration 180 Minutes
John E Lincoln
%
COMPLETE
$399
Learn the latest Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance Webinar
Available until
MP3 Download Duration 90 Minutes
Carolyn Troiano
%
COMPLETE
$199
A Culture of Quality is a Competitive Advantage
Available until
MP3 Download This webinar will cover FDA and NB expectations for Quality Systems , Best Practices and How culture can impact quality and compliance risk in 2021
Susanne Manz
%
COMPLETE
$199
Understanding the Design Verification and Validation Requirements for Medical Devices
Available until
MP3 Download Duration 60 Minutes
Meena Chettiar
%
COMPLETE
$199
Best Practices for Auditing a Vendor of Computer Systems Regulated by FDA
Available until
MP3 Download Duration 90 Minutes
Carolyn Troiano
%
COMPLETE
$199
Managing Compliance during the Pandemic
Available until
MP3 Download Duration 60 Minutes
Danielle DeLucy
%
COMPLETE
$199
21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
Available until
MP3 Download This webinar will help you understand in detail the application of FDA’s 21 CFR Part 11 guidance on electronic records
Carolyn Troiano
%
COMPLETE
$199
4-Hour Virtual Seminar - Batch Record Review and Product Release
Available until
MP3 Download Duration 240 Minutes
Danielle DeLucy
%
COMPLETE
$499
NEW FDA Proposed FSMA Rule on Food Traceability During COVID19 – New Course
Available until
MP3 Download Duration 60 Minutes
Dr. John M. Ryans
%
COMPLETE
$199
Properly Managing CAPA Programs for Successful Implementation
Available until
MP3 Download Duration 90 Minutes
Danielle DeLucy
%
COMPLETE
$199
Why people make mistakes. Understanding Human error
Available until
MP3 Download Duration 90 Minutes
Ginette Collazo
%
COMPLETE
$199
Clinical Data Management Training
Available until
MP3 Download Duration 2 Day
Elaine Eisenbeisz
%
COMPLETE
$1,699
Rouge Monitoring - The usage of science-based online instrumentation to determine derouging and pas
Available until
MP3 Download Duration 60 Minutes
Nissan Cohen
%
COMPLETE
$199
Webinar FDA’s Regulatory Management of Your Cybersecurity Threats
Available until
MP3 Download -Duration 60 Minutes
Casper (Cap) Uldriks
%
COMPLETE
$199
Masterclass: 4 Keys to Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations
Available until
MP3 Download Duration 120 Minutes
John G. Lanese
%
COMPLETE
$499
FDA’s Regulation Human Cellular Biologics including Preclinical and First-In-Human Considerations
Available until
MP3 Download Duration 90 Minutes
Karl M. Nobert
%
COMPLETE
$199
Learn the latest webinar Software Validation Utilizing Principles of Lean Documents and Lean Configuration
Available until
24-Feb,2021 at 01:00 PM ET | 10:00 AM PT | 12:00 PM CT Duration 90 Minutes
Jose Mora
%
COMPLETE
$199
Cybersecurity, Data Integrity, Part 11, and Required Software Validation
Available until
MP3 Download This online training describes FDA Guidances on Cybersecurity and Data Integrity , FDA’s enforcement, Software Validation , CGMPs and Cloud
John E Lincoln
%
COMPLETE
$399
Understanding the Design Verification and Validation Requirements for Medical Devices
Available until
MP3 Download Duration 60 Minutes
Meena Chettiar
%
COMPLETE
$199
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