Top Industry News
- FDA-Benefit-Risk Assessment for New Drug and Biological Products
- SWISS-HOMANT Asia Software available for the First time
- FDA-Electronic Submission Template for Medical Device 510(k) Submissions
- MHRA-Borderlines with medical devices and other Products in Great Britain
- ANVISA Publishes Manual on food Import
- CDSCO Shares Guide to Registering non-notified medical devices for Import, Production
- ANVISA Updates list of Documents for Petition for Evaluation of Enzymes and Probiotics
- MHRA Shares Guidance on Need to Review Registration of medical devices
- ANVISA-Open Consultation for Review of the Regulatory Impact Analysis Guide
- MHRA-Clinical trials for medicines: apply for Authorisation in the UK