We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Beginning this month, each issue of Drug GMP Report will include a four-page PharmaDevice IT Report supplement. So, in addition to the information on industry best practices and advice on drug manufacturing issues you’re used to getting with DGR, you will also receive information on FDA actions on Part 11 and other technology initiatives from the agency and other government offices.