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Kelly Thomas


FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control
Sep 26 This webinar will discuss the FDA requirements and guidelines for investigating Out-of-trend (OOT) results in the pharmaceutical
Kelly Thomas Kelly Thomas
$249
Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)
Sep 27-28 In this two day workshop conference you will learn the requirements and expectation
Kelly Thomas Kelly Thomas
$1,295
cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA
Oct 05 This webinar will cover the key areas of how ICH Q7 was established, it's goals and object
Kelly Thomas Kelly Thomas
$499
Quality Control Laboratory Compliance - cGMPs and GLPs Course - What Regulatory, Compliance & Quality Professionals Need to Know
Oct 26-27 This course will provide an overview of the Regulatory requirements governing QC Labs to ensure compliance with cGMP and GCP
Kelly Thomas Kelly Thomas
$1,299
Analytical Methods Validation for FDA Compliance
Nov 02-03 In this course, general guideline for the determination of the analytical
Kelly Thomas Kelly Thomas
$1,295
Investigating Out-of-Specification (OOS) Test Results in the Laboratory; FDA Guidance and Latest Expectations Training
Nov 14 The objective of this live training webinar is to develop an understanding
Kelly Thomas Kelly Thomas
$299
Writing Standard Operating Procedures (SOP) Course Online & Certificate for FDA-Regulated Industry
Dec 04-06 This course will address how to write effective Standard Operating Procedures and Work Instructions in support of company
Kelly Thomas Kelly Thomas
$1,295
FDA Recalls - Before You Start, and After You Finish
Dec 12-13 this seminar will help you to Understand FDA's recall authority and policy
Kelly Thomas Kelly Thomas
$1,495
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
$895
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
Kelly Thomas Kelly Thomas
$1,295
Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach
MP3 Download This eight-hour vendor qualification audit training will help you improve
Kelly Thomas Kelly Thomas
$1,199
GMP Auditing for Quality Assurance Training Course for FDA Regulated Industries
MP3 Download GMP Auditing for the Pharmaceutical Industry
Kelly Thomas Kelly Thomas
$1,495
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
$1,495
CROs (Clinical Research Organizations) - Identification, Selection, and Management for Maximum Results & Value
MP3 Download This course will provide the attendees with all the specific methodology and management techniques to successfully outsource pharmaceutical programs
Kelly Thomas Kelly Thomas
$1,495
Implementing a Robust and Compliant Change Control Program
MP3 Download This Change Control training program will discuss regulatory expectations from the FDA, EU and ICH perspective
Kelly Thomas Kelly Thomas
$229
FDA Recalls - Before You Start, and After You Finish
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 Kelly Thomas
€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
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
Quality Control Laboratory Compliance - cGMPs and GLPs
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
$1,495
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
Analytical Method Validation and Transfer
MP3 Download This course will provide a thorough review of regulatory guidelines on method validation and transfer
Kelly Thomas Kelly Thomas
$229
Annual Current Good Manufacturing Practices (cGMP) Training
MP3 Download This webinar provides a basic understanding and fundamental principles of Current Good Manufacturing Practices and will fulfill the requirement
Kelly Thomas Kelly Thomas
$229
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
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
$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