Bob McDowall
Bob has over twenty years experience working as an analytical chemist, including fifteen years experience within the pharmaceutical industry working for two multinational companies.
He is the author of over 900 scientific papers, presentations and posters on bioanalytical methods, analytical method validation, sample preparation, computerized system validation (including 21 CFR 11 electronic records and electronic signatures), laboratory automation and LIMS.
He was the only European co-chair and co-author of the first AAPS FDA meeting on Bioanalytical Method Validation in 1990.
More content by Bob McDowall
5 dangerous data integrity risks your lab may be taking
February 01 by Bob McDowallRegulatory authorities like the FDA and MHRA expect pharma labs to constantly improve how they safeguard drug quality. There are many data integrity risks for labs to combat
