Top Industry News
- FDA Finalizes Rule to Go From Paper to Electronic Device Submissions
- ANVISA- CTD Electronic Protocol Published
- SFDA- Guidance on Requirements for Unique Device Identification (UDI) for Medical Devices
- TGA- Guidance on the New Regulatory Requirements for IVD Companion Diagnostics
- EMA- How Will Pharmacovigilance Look in 2030?
- Finland Prepares for 2020 Introduction of new Clinical Trial Regulations
- ANVISA- New Standard on Sanitizer Registration Published