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Kelly Thomas


FDA Recalls - Before You Start, and After You Finish
On 11 - 12 May, 2021 this seminar will help you to Understand FDA's recall authority and policy , Learn how to manage recalls under FDA oversight.
Kelly Thomas Kelly Thomas
$1,599
Webinar Analytical Method Validation and Transfer According to the New FDA Guidance
20 May This course will prepare attendees with the knowledge and tools to plan and execute test method validation packages for the NDA
Kelly Thomas Kelly Thomas
$499
Establishing a Robust Data Integrity Program
25 May This webinar will detail a data integrity governance program and principles for defining quality and data integrity into processes and systems.
Kelly Thomas Kelly Thomas
$199
Establishing Appropriate Quality Metrics and Key Performance Indicators (KPIs)
03 June This course will discuss the importance of establishing metrics, how to distinguish Key Performance Indicators (KPIs)
Kelly Thomas Kelly Thomas
$199
Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
June 15-16 This 2-day seminar will explain the new Analytical Procedure Lifecycle guidelines and give attendees the knowledge needed to implement recommend
Kelly Thomas Kelly Thomas
$1,599
Root Cause Analysis Techniques and CAPA Management
7 July This webinar will give you a systematic approach that utilizes quality tools to objectively identify factors that have resulted in or could contribute to
Kelly Thomas Kelly Thomas
$299
What do the FDA, EMA and PMDA Look for When Conducting cGMP Regulatory Inspections
04 Aug 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 Kelly Thomas
$299
3 Hrs Virtual Webinar on Aseptic Processing and Validation
02 Sep This course will provide an overview of requirements for aseptic and bulk manufacturing operations, including facility design and contamination
Kelly Thomas Kelly Thomas
$299
Post-Market Activities in the EU-MDR — A Detailed Analysis
MP3 Download Medical device training will review the new EU-MDR requirements governing Post Market Activities and discuss quality system approaches
Kelly Thomas Kelly Thomas
$399
Quality Control Laboratory Compliance - cGMPs and GLPs
MP3 Download Duration 2 Day
Kelly Thomas Kelly Thomas
$1,895
Data Integrity Practices for the Laboratory and Beyond
MP3 Download -Duration 90 Minutes
Kelly Thomas Kelly Thomas
$199
Upgrade Your Medical Device Recall Strategy
MP3 Download Duration 90 Minutes
Kelly Thomas Kelly Thomas
$199
Meeting Global Unique Device Identification Requirements
MP3 Download Duration 90 Minutes
Kelly Thomas Kelly Thomas
$199
Pharmaceutical Quality Risk Management
MP3 Download Duration 90 Minutes
Kelly Thomas Kelly Thomas
$249
EU MDR Implementation and Transitioning to the Deadline: Essential Tasks to Complete
MP3 Download Duration 360 Minutes
Kelly Thomas Kelly Thomas
$799
Understanding the Drug Supply Chain Security Act: Latest Regulatory Developments and Best Practices
On Demand Webinar Duration 90 minutes
Kelly Thomas Kelly Thomas
$289