ComplianceOnline

Expert Profile


Gregory Martin
Founder and President, Complectors Consulting LLC.

is the founder and President of Complectors Consulting LLC, which provides consulting and training in the area of Pharmaceutical Analytical Chemistry. Greg is Vice Chair of the USP General Chapters Expert Committee, and has over 29 years experience in the pharmaceutical industry, including ten years as Director of Pharmaceutical Analytical Chemistry in Merck Research Laboratories. Greg's interests include impurities and residual solvents, dissolution, analytical instrument qualification and other topics related to laboratory GMP compliance.

Trainings by Expert

Lifecycle Approach to Analytical Methods with QbD Elements: Design, Development, Validation, Transfer
Category: Drugs and Chemicals (Pharma) , Quality and Safety , Supply Chain and Manufacturing , Life sciences QA/QC , Life Sciences , QA/QC

Residual Solvents: Understanding the Requirements and Practical Advice for Implementing USP <467>/ICH Q3C
Category: Drugs and Chemicals (Pharma) , Quality and Safety , Supply Chain and Manufacturing , Life Sciences

Dissolution Instrument Qualification to Meet Requirements and Minimize Product OOS Dissolution Results
Category: Drugs and Chemicals (Pharma) , Testing and Validation , Quality and Safety , Laboratory , Life Sciences

4-hr Virtual Seminar: Using the USP Effectively
Category: Laboratory Compliance , Quality and Safety , Laboratory , Contamination Control , Life Sciences

QbD Approach to Analytical Method Lifecycle: Design, Development, Validation, Transfer
Category: Drugs and Chemicals (Pharma) , Quality and Safety , Drug Development , Life sciences QA/QC , Research & Development , Drug R & D , Life Sciences , QA/QC

Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results
Category: Laboratory Compliance , Testing and Validation , Quality and Safety , Laboratory , Life Sciences

Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory
Category: Drugs and Chemicals (Pharma) , Laboratory Compliance , All FDA Regulated Industry , Quality and Safety , Audits & Inspections , Laboratory , GLP & Other Best practices , Microbiology Laboratory , Drugs Regulations , Biotech Regulations , Audit & Inspection-Role , Lab Audit , Life sciences QA/QC , Best Practices & GXPs , Life Sciences , Regulatory Affairs , Common FDA Regulations , QA/QC

Regulatory Readiness in 2013 - Comprehensive Compliance Training Package for Pharma Companies (8 Courses)
Category: Drugs and Chemicals (Pharma)

USP Hot Topics: What's Hot Now and How to Track Coming Changes and Influence USP
Category: Drugs and Chemicals (Pharma) , Laboratory Compliance , Laboratory Compliance , Quality and Safety , Audits & Inspections , Laboratory , Drug Development , Drugs Regulations , Audit & Inspection-Role , Lab Audit , Drugs Inspections , Life sciences QA/QC , Research & Development , Drug R & D , Regulations & Guidances , Life Sciences , Regulatory Affairs , QA/QC

Lean Approaches to Development of HPLC Methods for Drug Products
Category: Laboratory Compliance