Top Industry News
- ANIVISA Check Out the New Subject Codes for Drug Labeling
- MHRA Regulating Medical Devices in the UK
- SWISS HOMANT Asia Software for the Approval of Asian Medicinal Products Without an Indication Based on a Notification (Notification Procedure)
- PMDA About Humanitarian Clinical Trials
- MHRA Medical Devices: Software Applications (apps)
- MHRA Guidance on Class I Medical Devices
- MHRA Medical Devices: Legal Requirements for Specific Medical Products
- MHRA Medical Devices Regulations: Compliance and Enforcement
- MHRA Virtual Manufacturing of Medical Devices
- MHRA Borderlines with Medical Devices and Other Products in Great Britain
- Washington State’s Toxic-Free Cosmetics Act Passes House of Representatives, Moves to Senate
- East African Standard 1119-4: 2023 on Skin Applied Mosquito Repellents – Specification (Part 4): Bathing Soap
- EU Commission Proposes Restrictions on D4, D5 and D6 in Consumer and Professional Products
- In New Zealand Public Health Message Released in Accordance with Section 24(f) of the Smoke Free Environments and Regulated Products Act 1990
- BASF SE Drops Appeal as European Chemicals Agency Corrects Decision on o-Xylene Testing Proposal
- Peru Released Decree on the Implementation of the National Chemical Management Framework
- Therapeutic Goods (Permissible Ingredients) Determination (No. 3) 2023: Updates and Clarifications for Medicinal Ingredients
- Ministry of Food and Drug Safety Introduces Measures to Enhance Oversight of Overseas Direct Purchases and Streamline Import Inspections