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Kelly Thomas


Courses

Analytical Method Validation, Verification & Transfer – FDA & ICH Compliance Training (2 Day)
July 20-21 | Sep 09-10 This training provides a practical, step-by-step approach to analytical method validation, verification, and transfer.
Kelly Thomas Kelly Thomas
$1,295
Efficient Batch Record Design & Review Training
July 22-23 In this accredited training, we will identify and discuss Master Batch Records (MBR), regulatory requirements, and key steps for issuance, batch record review, reconciliation, and final QA disposition
Kelly Thomas Kelly Thomas
$1,450
FDA Inspection Readiness in the AI Era 2026
July 22-23, 2026, Time 12:30pm-5:00pm EST Understand how FDA AI-driven targeting may impact inspections
Kelly Thomas Kelly Thomas
$1,199
cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA
Jul 23 This webinar will cover the key areas of how ICH Q7 was established, it's goals and object
Kelly Thomas Kelly Thomas
$495
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.
Kelly Thomas Kelly Thomas
$5,995
The Drug Development Process from Concept to Market - 20 Hrs Course
Aug 10-13 Time 12:00 PM – 05:00 PM ET Gain a complete understanding of the drug development process from concept to market in this 4-day virtual training, covering key stages from discovery and preclinical research to clinical trials and regulatory approval aligned with the U.S. Food and Drug Administration.
Kelly Thomas Kelly Thomas
$1,495
Writing Effective SOPs & Process Documents: Meet Regulatory Requirements and Ensure GMP Compliance
Aug 11-13, 2026, This course will address how to write effective Standard Operating Procedures and Work Instructions in support of company
Kelly Thomas Kelly Thomas
$1,495
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies 20 hrs Course
Aug 17-20, Time 12:00 PM – 05:00 PM ET Gain the confidence to navigate Good Laboratory Practice (GLP nonclinical) requirements with this practical online training designed for today’s laboratory professionals, aligned with OECD GLP principles and expectations from global regulators like the U.S. Food and Drug Administration and European Medicines Agency.
Kelly Thomas Kelly Thomas
$5,995
Practical ICH Q10 Pharmaceutical Quality System (PQS) Implementation Training
Aug 26-27 Participants will gain a comprehensive understanding of the ICH Q10 model, Quality Risk Management (ICH Q9(R1)), CAPA, Change Management, Supplier Quality Management, Process Performance and Product Quality Monitoring, Management Review, and Inspection Readiness.
Kelly Thomas Kelly Thomas
$1,295
Implementing an FDA Compliant Stability Program
July 29-30 This practical, expert-led training provides a complete, real-world understanding of how to design, implement, and defend an FDA-compliant
Kelly Thomas Kelly Thomas
$1,495
GMP Auditing for Quality Assurance Training Course for FDA Regulated Industries
MP3 Download GMP Auditing for the Pharmaceutical Industry
Kelly Thomas Kelly Thomas
$1,295
Supplier and Contract Manufacturer Management
MP3 Download This 2-day course will cover managing a supplier for the entire lifecycle of the relationship, beginning with identification and qualification. Participants will receive a Professional Certificate with 10 hours of Continuing Education aligned with Supplier Management
Kelly Thomas Kelly Thomas
$1,295
2 Day Virtual Seminar Quality Control Laboratory Compliance Training – cGMP, GLP and FDA Requirements
MP3 Download 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 Kelly Thomas
$1,450
Supplier Audits & Vendor Qualification Training: Avoid FDA 483s and Ensure GMP Compliance
MP3 Download This eight-hour vendor qualification audit training will help you improve
Kelly Thomas Kelly Thomas
$1,295
FDA Inspections 2 Day Virtual Seminar Online
MP3 Download This 10-hour seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter. FDA inspections courses provide essential training on GMP compliance, inspection readiness, and interaction with FDA investigators, featuring topics like 483 responses and mock audits. Time 12:00 PM – 05:00 PM ET | 09:00 AM - 02:00 PM PT (US) Participants will receive a Professional Certificate with 10 hours of Continuing Education aligned with FDA Inspection
Kelly Thomas Kelly Thomas
$1,295
FDA Recalls - Before You Start, and After You Finish
MP3 Download - 12:00 pm – 05:00 PM EST Join our 2-day online FDA Recalls course online to learn proactive strategies for recall preparation and post-recall compliance.
Kelly Thomas Kelly Thomas
$1,295
Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations Training
MP3 Download The objective of this live training webinar is to develop an understanding
Kelly Thomas Kelly Thomas
$299
FDA Root Cause Analysis & CAPA Training for Pharma & Medical Device Professionals
MP3 Download
Kelly Thomas Kelly Thomas
$5,995
FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control
MP3 Download This webinar will discuss the FDA requirements and guidelines for investigating Out-of-trend (OOT) results in the pha
Kelly Thomas Kelly Thomas
$199
Pharmaceutical Document Management Training Course - A Global Regulatory Approach
MP3 Download This course is designed for individuals responsible for documentation writing and management in the pharmaceutical and related industries
Kelly Thomas Kelly Thomas
$1,895
Quality Control Laboratory Compliance - cGMPs and GLPs Course - What Regulatory, Compliance & Quality Professionals Need to Know
MP3 Download This course will provide an overview of the Regulatory requirements governing QC Labs to ensure compliance with cGMP and GCP
Kelly Thomas Kelly Thomas
$1,295
Basic GMP Training for the QC Laboratory
MP3 Download This course will provide participants with an understanding of how to effectively handle out-of-specification
Kelly Thomas Kelly Thomas
$1,295
Establishing Appropriate Quality Metrics and Key Performance Indicators (KPIs)
MP3 Download This course will discuss the importance of establishing metrics, how to distinguish Key Performance Indicators (KPIs)
Kelly Thomas Kelly Thomas
$189
Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)
MP3 Download In this two day workshop conference you will learn the requirements and expectation
Kelly Thomas Kelly Thomas
$1,843
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.
Kelly Thomas Kelly Thomas
$1,495
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
Kelly Thomas Kelly Thomas
$3,999
3 Hrs Virtual Webinar on Aseptic Processing and Validation
MP3 Download This course will provide an overview of requirements for aseptic and bulk manufacturing operations, including facility design and contamination
Kelly Thomas Kelly Thomas
$299
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
Kelly Thomas Kelly Thomas
€1.295
Establishing a Robust Data Integrity Program
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 Kelly Thomas
$199
Webinar Analytical Method Validation and Transfer According to the New FDA Guidance
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 Kelly Thomas
$499
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
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
Understanding the Drug Supply Chain Security Act: Latest Regulatory Developments and Best Practices
On Demand Webinar Duration 90 minutes
Kelly Thomas Kelly Thomas
$289