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Medical device Training (84)
FDA Regulatory Compliance Training (234)
Pharma Courses & Pharmaceutical Training (209)
Biotechnology Online Courses and Training (186)
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Virtual Seminars (61)
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Europe Seminars (31)
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Author:
Kelly Thomas
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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
Eleonora Babayants
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
Find a product
Kelly Thomas
Analytical Method Validation, Verification and Transfer
Available until
June 30 & July 01 In this course, general guideline for the determination of the analytical characteristics for different types of validation procedures
Kelly Thomas
%
COMPLETE
$1,498
FDA Recalls - Before You Start, and After You Finish
Available until
July 06-07 this seminar will help you to Understand FDA's recall authority and policy , Learn how to manage recalls under FDA oversight.
Kelly Thomas
%
COMPLETE
$2,995
EU MDR Implementation and Transitioning to the Deadline: Essential Tasks to Complete
Available until
July 21-22 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
Kelly Thomas
%
COMPLETE
$755
Basic GMP Training for the QC Laboratory
Available until
July 27-28 This course will provide participants with an understanding of how to effectively handle out-of-specification
Kelly Thomas
%
COMPLETE
$1,295
Implementing a Robust and Compliant Change Control Program
Available until
Aug 04 This Change Control training program will discuss regulatory expectations from the FDA, EU and ICH perspective
Kelly Thomas
%
COMPLETE
$229
FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control
Available until
MP3 Download This webinar will discuss the FDA requirements and guidelines for investigating Out-of-trend (OOT) results in the pharmaceutical laboratory
Kelly Thomas
%
COMPLETE
$229
Analytical Method Validation and Transfer
Available until
MP3 Download This course will provide a thorough review of regulatory guidelines on method validation and transfer
Kelly Thomas
%
COMPLETE
$229
Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
Available until
MP3 Download This 2-day seminar will explain the new Analytical Procedure Lifecycle guidelines and give attendees the knowledge needed to implement recommend
Kelly Thomas
%
COMPLETE
$1,495
A Comprehensive View of Medical Device Post-Market Regulations and Challenges During COVID-19— Complaint Handling, MDR Reporting and Recalls
Available until
MP3 Download This course will explain how to comply with complicated Complaint Handling, MDR and Recall requirements. Earl Bird. Register.
Kelly Thomas
%
COMPLETE
$1,495
FDA Recalls - Before You Start, and After You Finish
Available until
MP3 Download this seminar will help you to Understand FDA's recall authority and policy , Learn how to manage recalls under FDA oversight.
Kelly Thomas
%
COMPLETE
€1.595
Navigating the Medical Device Post-Market Maze and Challenges during COVID-19 Pandemic - Learn what FDA is really thinking on regulation and guidance documents
Available until
MP3 Download this course will explain how to comply with complicated Complaint Handling, MDR and Recall requirements. Earl Bird. Register.
Kelly Thomas
%
COMPLETE
$1,495
Quality Control Laboratory Compliance - cGMPs and GLPs
Available until
Aug 11-12 This course will examine the fundamental requirements for all QC laboratories subject to FDA inspection, recent trends from FDA inspection reports and enforcement actions
Kelly Thomas
%
COMPLETE
$1,495
Annual Current Good Manufacturing Practices (cGMP) Training
Available until
MP3 Download This webinar provides a basic understanding and fundamental principles of Current Good Manufacturing Practices and will fulfill the requirement
Kelly Thomas
%
COMPLETE
$229
3 Hrs Virtual Webinar on Aseptic Processing and Validation
Available until
MP3 Download This course will provide an overview of requirements for aseptic and bulk manufacturing operations, including facility design and contamination
Kelly Thomas
%
COMPLETE
$299
What do the FDA, EMA and PMDA Look for When Conducting cGMP Regulatory Inspections
Available until
MP3 Download This webinar will cover the key areas of how ICH Q7 was established, it's goals and objectives, expectations of the healthcare authorities
Kelly Thomas
%
COMPLETE
$499
Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
Available until
MP3 Download This 2-day seminar will explain the new Analytical Procedure Lifecycle guidelines and give attendees the knowledge needed to implement recommend
Kelly Thomas
%
COMPLETE
€1.295
Establishing a Robust Data Integrity Program
Available until
MP3 Download This webinar will detail a data integrity governance program and principles for defining quality and data integrity into processes and systems.
Kelly Thomas
%
COMPLETE
$199
Establishing Appropriate Quality Metrics and Key Performance Indicators (KPIs)
Available until
MP3 Download This course will discuss the importance of establishing metrics, how to distinguish Key Performance Indicators (KPIs)
Kelly Thomas
%
COMPLETE
$199
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
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
Data Integrity Practices for the Laboratory and Beyond
Available until
MP3 Download -Duration 90 Minutes
Kelly Thomas
%
COMPLETE
$199
Upgrade Your Medical Device Recall Strategy
Available until
MP3 Download Duration 90 Minutes
Kelly Thomas
%
COMPLETE
$199
Meeting Global Unique Device Identification Requirements
Available until
MP3 Download Duration 90 Minutes
Kelly Thomas
%
COMPLETE
$199
Pharmaceutical Quality Risk Management
Available until
MP3 Download Duration 90 Minutes
Kelly Thomas
%
COMPLETE
$249
Understanding the Drug Supply Chain Security Act: Latest Regulatory Developments and Best Practices
Available until
On Demand Webinar Duration 90 minutes
Kelly Thomas
%
COMPLETE
$289