iPharMed, a European based service-oriented company offering regulatory solutions for Pharmaceuticals and Medical devices. Founded by a team of professionals with three decades of experience in the Pharm and Med Device industry. iPharMed will support beyond commitment and delivering Regulatory Services with flexibility, quality, speed with cost effective model. iPharMed effectively uses its infrastructure and talent to reduce the product registration time and also maintaining the post approval regulatory compliance. We are specialised in the Pharmaceuticals (CMC, eCTD and Pharmacovigilance) and Medical Devices (CER, BER, CE, 510(K) and PMS) area where we can provide complete End to End support iPharMed will help clients in the areas like IP, R&D, Quality, Sourcing of API & Products, Cosmetic and Consumer product registrations.