Speaker Profile

Greg
Greg Martin
President , Complectors Consulting LLC,

Greg Martin is President of Complectors Consulting (www.complectors.com) which provides consulting and training in the area of Pharmaceutical Analytical Chemistry. He has over 25 years experience in the pharmaceutical industry and was Director of Pharmaceutical Analytical Chemistry (R&D) for a major Pharma company for a number of years.

In addition, he has volunteered for the USP for over 10 years, and currently serves on the General Chapters - Chemical Analysis Expert Committee, and serves on Expert Panels on Validation and Verification, Residual Solvents and Use of Enzymes for Dissolution Testing of Gelatin Capsules.

He has particular interest in QbD/Lean approaches to dissolution testing, impurity methods, method lifecycle (development/validation/transfer) and instrument qualification, and is passionate about using good science and sound logic to achieve high quality results, consistent with cGMPs, while minimizing resources.

Mr. Martin is author of several papers in the areas of dissolution and analytical method validation, and is past chair of the AAPS In Vitro Release and Dissolution Testing Focus Group.

Upcoming Webinars Recorded Webinars
  • 18
  • December
  • 2020
  • Friday
10:00 AM PST | 01:00 PM EST

Understanding and Applying ICH Q3A and Q3B for Control of Impurities in Drug Substances and Drug Products

This course is designed to provide participants with an understanding of the regulatory expectations for controlling impurities and degradants (including DNA reactive/potential genotoxic impurities) in drug substances and drug products. There will be ample opportunity to discuss questions and challenges from the participants.

Greg Martin Greg Martin | Duration:90 Minutes | Price: $149.00 | View Details
Greg Martin

Understanding and Applying ICH Q3A and Q3B for Control of Impurities in Drug Substances and Drug Products

This course is designed to provide participants with an understanding of the regulatory expectations for controlling impurities and degradants (including DNA reactive/potential genotoxic impurities) in drug substances and drug products. There will be ample opportunity to discuss questions and challenges from the participants.

Speaker: Greg Martin | View Anytime | Duration: 90 Minutes | Price: $199.00 | View Details
Greg Martin

Understanding and Applying ICH Q3A and Q3B for Control of Impurities in Drug Substances and Drug Products

This course is designed to provide participants with an understanding of the regulatory expectations for controlling impurities and degradants (including DNA reactive/potential genotoxic impurities) in drug substances and drug products. There will be ample opportunity to discuss questions and challenges from the participants.

Speaker: Greg Martin | View Anytime | Duration: 90 Minutes | Price: $399.00 | View Details