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Top Industry News
- MHRA Guidance on New International Recognition Procedure
- MHRA Common Specification Requirements For In Vitro Diagnostic Devices
- SFDA Guidelines for Bioequivalence
- MHRA Announces a Proposed Framework for International Recognition of Medical Devices
- Recently The Food Safety Authority of Ireland Outlines Legislative Requirements for Food Supplements, Focusing on Flavouring Regulations, Labelling Requirements, and Nutrition and Health Claims
- ANVISA Published New Regulatory Framework for Medicinal Gases
- The Proposal Sought to Amend the Australia New Zealand Food Standards Code to Recognize Honey from Australian Native Stingless Bees as a Standardized Food
- EMA Medical Devices: New Guidance for Industry and Notified Bodies
- EU REACH Restriction on D4/D5/D6 Published
- SFDA Recognized Standards(Supporting Medical Device Premarket Submissions)
- European Medicines Network Designated as WHO Listed Authority
- MDA Public Comment Draft Guidance Document Change Notification For Registered Medical Device
- The Office for Product Safety and Standards (OPSS) is Conducting a Survey to Assess the Impact of an Upcoming Amendment to Annex III of the UK Cosmetics Regulation, Which Would Restrict Kojic Acid as a Cosmetic Ingredient Under Annex III
- California - Proposed Amendments for Titanium Dioxide under Proposition 65
- ANVISA Medical Devices: Webinar Will Deal with Petitions Through the Optimized Route
- AICIS has Issued Two Infringement Notices Totaling $37,560 to an Australian Importer of Fragrance, Toiletries, and Cleaning Products
- MHRA Announces Consultation on Improved Safety for High Risk In Vitro Diagnostic Devices