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Kelly Thomas


Courses

Efficient Batch Record Design & Review Training: GMP Compliance & FDA Requirements
May 07-08 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 Seminar
May 06-07 This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter
Kelly Thomas Kelly Thomas
$1,450
Supplier and Contract Manufacturer Management
May 20-21 This 2-day course will cover managing a supplier for the entire lifecycle of the relationship, beginning with identification and qualification
Kelly Thomas Kelly Thomas
$1,449
Quality Control Laboratory Compliance - cGMPs and GLPs
May 20-21 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
Analytical Methods Validation for FDA Compliance
June 03-05 In this course, general guideline for the determination of the analytical
Kelly Thomas Kelly Thomas
$1,895
FDA Recalls - Before You Start, and After You Finish
July 29-30 This seminar will help you to Understand FDA's recall authority and policy
Kelly Thomas Kelly Thomas
$1,495
Writing Standard Operating Procedures (SOP) Course Online & Certificate for FDA-Regulated Industry
Aug 05-07 This course will address how to write effective Standard Operating Procedures and Work Instructions in support of company
Kelly Thomas Kelly Thomas
$1,895
Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach
Aug 26-28 This eight-hour vendor qualification audit training will help you improve
Kelly Thomas Kelly Thomas
$1,895
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
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
$195
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
$295
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
cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA
MP3 Download This webinar will cover the key areas of how ICH Q7 was established, it's goals and object
Kelly Thomas Kelly Thomas
$595
Good Manufacturing Practices (GMP) Online Course
MP3 Download Our 4 Half-days long GMP training will equip you to increase your efficiency and strengthen your skills for a stellar career in the industry. Whether you want to level up your designation or become an entrepreneur, the credibility of a GMP course will only add stars to your portfolio.
Kelly Thomas Kelly Thomas
$1,995
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