At Complectors, we offer an approach to consulting in the area of Pharmaceutical Analytical Chemistry that is focused on solutions and implementation, not just identification of gaps. In addition, we can provide highly-interactive training on several topics related to pharmaceutical analysis in both live course and webinar formats. The training can be presented for your company (which is a very effective and cost-sparing way to train a group of individuals). Training is also offered in conjunction with several scientific meetings and by select course providers.
Greg Martin, President
Greg Martin 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 has over 25 years experience in the pharmaceutical industry and was Director of Pharmaceutical Analytical Chemistry (R&D) for a major PhRMA company for a number of years. In addition, he has volunteered for the USP for over 10 years, and currently serves as Vice Chair of the General Chapters – Physical Analysis Expert Committee, and serves on Expert Panels on Validation and Verification, Weights and Balances, Residual Solvents and Use of Enzymes for Dissolution Testing of Gelatin Capsules. He is also Chair of the AAPS In Vitro Release and Dissolution Testing Focus Group. Mr. Martin is co-author (with Vivian A. Gray) of the series “Dissolution Concepts and Applications” which has appeared in Journal of Validation Technology and Journal of GXP Compliance. He can be contacted at email@example.com.