RADAYDRUG Ltd was established in 1998 by pharmaceutical professionals with the aim of becoming a distinguished service provider across key areas of the pharmaceutical and medtech industries.
We offer comprehensive support throughout the development and entire lifecycle of medicinal products and medical devices.
Pharmacovigilance, Study safety and Medical services:
Full pharmacovigilance services, PV system building, maintenance, audits
Comprehensive pharmacovigilance support throughout product lifecycle
Your global partner to manage safety activities of clinical trials
Pharma R&D, Regulatory Affairs:
Clinical trial operations
Medical writing
Dossier building
Support in preparation of manufacturing files, CMC development
Registration and lifecycle management
Medical Device:
Certification management in EU
Technical file building, clinical evaluation
Post marketing support: surveillance, vigilance, dossier maintenance
Over the years, we have attracted numerous talented and dedicated experts, accumulating extensive experience and knowledge. This expertise has been consolidated into a regulatory, R&D, and pharmacovigilance knowledge center, serving clients in the pharmaceutical and medtech sectors — including manufacturers, developers, sponsors of clinical studies and distributors of pharmaceuticals, medical devices, cosmetics, and food supplements.
The high quality of our services is also guaranteed by our comprehensive and integrated quality assurance system, which complies with the relevant GxP guidelines and the requirements of the ISO 9001 standard.