EUROPEAN MEDICINES AGENCY POST-AUTHORISATION ADVICE 2026
Europe, Jan 17 2025 – The European Medicines Agency (EMA) published its latest post-authorisation procedural advice (Revision 116) on January 15, 2026. While primarily focused on medicinal products, this guidance significantly impacts medical device manufacturers, particularly those producing integral devices for combination products or medicinal products with ancillary device components. The new guidance introduces critical […]
INDIAN DENTAL IMPLANT MARKET: REGULATIONS, COMPETITION, AND HOW TO ENTER
INTRODUCTION The dental implant market world is shifting. While markets in North America and Western Europe are getting crowded, medical device companies are turning their attention to the fast-growing Asia-Pacific (APAC) region. In this mix, India isn’t just a “maybe”—it is becoming a major player that will likely change how dental care is consumed in […]