Top Industry News
- Republic of Cyprus - Implementation of ISO standards for the identification of medicinal products – IDMP
- Health Canada’s Intention to Adopt the Use of the Table of Contents Format for Class III and IV Premarket Medical Device Licence Applications
- Republic of Cyprus - Implementation of Commission Delegated Regulation (EU) 2016161 - Safety Features appearing on the packaging of medicinal products for human use
- MHRA- Clinical trials for medicines: apply for authorisation in the UK (updated)
- DMA- Companies can now apply for authorisation to produce cannabis bulk and cannabis primary products
- FDA- Microdose Radiopharmaceutical Diagnostic Drugs: Nonclinical Study Recommendations
- MHRA- Good laboratory practice (GLP) for safety tests on chemicals (updated)