Regulatory Advice & Expertise

We are proud supporters of the biopharma industry by offering our services in the development of effective drugs and medical devices. We provide a range of regulatory operational resources for clinical and medical services in the global market. From clinical trial study design and analyses to training, submission reports and publications, R-S-S uses its network of clinical and medical experts to support clients on every step of their journey. We offer consultancy to the biopharma industry and conduct continuous assessments on the ever-changing regulatory requirements in industry.

 

Areas of Expertise

  • Clinical Studies Design Assistance

  • Clinical Trial Applications (CTA)

  • New Drug Applications & Submissions

  • Market Authorisation Applications

  • Data Management

  • Clinical Trial and Information Systems (CTIS)

  • Applications and Submissions Quality Control

  • Medical Report Writing

  • Clinical Expertise 

  • Disease Area Expertise

 

Contact us for more information