Previous Blogs


By Janet Gaboury, PhD

October 21, 2019

West Regulatory Affairs (RA) has a goal of harmonizing site-specific Drug Master Files (DMFs) into a global document as the processes at different facilities are synchronized.


By Stephen LoCastro

May 18, 2017

Both the FDA and Health Canada have issued guidances to industry that require Drug Master Files (DMFs) to be provided in electronic formats by defined deadlines.