Top Industry News
- Health Canada-Implementation of Regulated Product Submission (RPS) and Electronic Common Technical Document version 4 (eCTD v4)
- MCC-Post-Marketing reporting of ADRs to Human Medicines in South Africa showing changes
- Regulators in EU, Japan and US take steps to facilitate development of new antibiotics
- DMA-New format requirements for marketing authorisation applications
- MCC-Amendments guideline for Biological Medicines
- Application of EU clinical trial regulation delayed to 2019
- Top 10 global CROs 2017