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Top Industry News
- MHRA Public Consultation on the Proposal to Make Codeine Linctus Available as a Prescription-Only Medicine (POM)
- ANVISA - Companies Must Submit a Drug Marketing Report
- PMDA - Publication of Foreign Manufacturer Certification/Registration Number
- ANVISA Medical Device Traceability Labeling is the Patient's Right. Know More
- MDA Medical Device Authority Media Statement Medical Device Authority (MDA) Ministry Of Health Malaysia
- TGA - Medicines Product Information Safety Updates
- ANVISA joins the OAS-Integrated Program
- CE/EFfCI Joint Guidance Unveils Practical Insights on EU REACH Microplastics Restriction: Requirements, Decision-Making Process, FAQs, and Legal Interpretations Provided for Industry Compliance
- Draft Standard Unveils New Labeling Requirements for Prepackaged Foods in China: Highlights on Definitions, Digital Labels, Food Claims, Shelf Life, and Allergenic Substances; Public Comments Accepted Until April 16, 2024
- Japan's Ministry of Agriculture, Forestry, and Fisheries (MAFF) Implements Revisions to Carbonated Beverage Standards, Expanding Scope and Incorporating New Requirements for Raw Materials
- FDA Fraudulent and Unreliable Laboratory Testing Data in Premarket Submissions: FDA Reminds Medical Device Manufacturers to Scrutinize Third-Party-Generated Data
- CTPA Addresses Labeling of Allergens Formed by Reactions in Products, Highlighting SCCS Opinion on Fragrance Allergens; Emphasizes Compliance with EU Regulations and Labelling Requirements
- FDA Select Updates for the Medical Device User Fee Small Business Qualification and Certification Guidance
- Draft Standard Proposes Revisions to China's National Food Safety Standard for Supplementary Food Nutritional Supplements, Including Scope, Terminology, and Inspection Methods; Public Comments Accepted Until April 12, 2024