Mr. Kuhn was trained as an analytical chemist at SUNY Geneseo. He began his career in the pharmaceutical industry at Merck Manufacturing Quality Operations in 1998 where he worked in several laboratory and validation capacities. After five years in the cGMP area, he has spent six years in Clinical Quality Assurance roles at Eisai, sanofi-aventis, and most recently at Celgene where serves as Clinical Quality Assurance with a focus on computer systems and vendor audits.
T. J. Kuhn | GxP Zone 
Dear Mr. Kuhn, I am looking for the link on the FDA website that has information regarding ALCOA with regards to Good Clinical Practice. The previous links are no longer active. Thank you.
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