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Top Industry News
- FDA - Reporting Amount of Listed Drugs and Biological Products Technical Conformance Guide
- MHRA UK Approved Bodies for Medical Devices
- MHRA Publishes New Guidance to Help Applicants and Shorten Timeframes for Assessment of Established Medicines
- MHRA updated the Guidance on Apply for a Licence to Market a Medicine in the UK
- EAEU in Russia Implements Key Amendments to Customs Union Regulations on Food Additives and Flavorings, Reducing Permitted Additives and Introducing New Standards
- MHRA Guidance on Established Medicines Marketing Authorisation Application (MAA) Process Changes
- PMDA - Medical Safety Measures Related to Pharmaceuticals and Medical Devices
- PMDA - Information on Risks, etc. Under Evaluation Regarding Regenerative Medicine Products
- American Cleaning Institute Urges Regulatory Clarity in Response to New York's Proposed 1,4-Dioxane Limits, Advocates for Industry Compliance Safeguards and Technical Refinements
- PMDA - Information on Risks, etc. Under Evaluation Regarding Pharmaceuticals
- FDA Draft guidance - Key Information and Facilitating Understanding in Informed Consent Guidance for Sponsors, Investigators, and Institutional Review Boar
- French Health Agency ANSES Declares Melamine Toxic to Reproduction, Sparking Heightened Concerns Over its Presence in Food-Contact Products
- FDA and Industry Collaborative Effort Halts Sales of PFAS in US Food Packaging, Marking a Significant Milestone for Public Health Protection
- MHRA The Innovative Devices Access Pathway (IDAP) - Pilot Phase
- European Union Reaches Provisional Agreement on Overhauling 'Breakfast Directives' for Honey, Fruit Juices, Jams, and Dehydrated Milk, Introducing New Information and Manufacturing Requirements
- ECHA Achieves 20% Compliance Check Milestone for REACH Registration Dossiers, Emphasizes Continued Focus on Chemical Safety in the European Union