1 USFDA’s new improvements to electronic medical device reporting(eMDR) freyrsolutions.com freyr solutions 3 years ago in Business 0
1 FDA’s final guidance on multiple function device products freyrsolutions.com freyr solutions 3 years ago in Technology 0
1 FDA's ANDA stage wise submission criteria to avoid Refuse to Receive, RTR freyrsolutions.com freyr solutions 5 years ago in Business 0
1 FDA's New Amendment, ‘Deemed to be licenced’ as Biologics freyrsolutions.com freyr solutions 5 years ago in Business 0
1 Cosmetics labeling requirements, US, Europe, China, Australia, India, Korea freyrsolutions.com freyr solutions 5 years ago in Business 0
1 Effective IND Application Submission Process and Components Involved freyrsolutions.com freyr solutions 5 years ago in Business 0
1 Manufacturing site change supplement guidance from FDA, PMA, Medical devices freyrsolutions.com freyr solutions 5 years ago in Business 0
1 Prerequisites for BLA approval process, BLA submissions, FDA 356h, biologics freyrsolutions.com freyr solutions 5 years ago in Business 0
1 Clean labels, Regulations, clean label products, Europe, USA, food products freyrsolutions.com freyr solutions 5 years ago in Business 0
1 Personal Care Products Safety Act, USA, FDA freyrsolutions.com freyr solutions 5 years ago in Business 0