Top Industry News
- FDA Providing Regulatory Submissions in Electronic and Non-Electronic Format—Promotional Labeling and Advertising Materials for Human Prescription Drugs
- TGA Medical device application processing times
- FDA issues MAPP on complex product classification for generic development
- Ireland’s HPRA simplifies labeling mock-up review procedure to accelerate licensing
- Malaysia’s MDA posts draft guidance on medical device change notifications
- EMA shares draft guidance on protecting confidential data in CTIS
- SFDA Requirements of Importation and Re-Exportation for Radioactive Materials Used in Medical Applications (MDS-REQ6)
- Pakistan’s DRAP consults public about guidance on applying to run clinical trials