CliniCan Health Research provides regulatory and clinical study/trial management services to pharmaceutical and biotechnology companies. We also extend our services to scientific/medical writing, designing effective research and development plans, SOPs and protocol development, licensing, marketing and post-market support as a CRO. We take pride to perform these core services with authority. Our very experienced team of scientific and medical experts are committed to bring the entire clinical research services to the next level; we believe in making it easy and making it right for our clients. We are committed to provide best of service our customers need. Please Contact Us to discuss the opportunity to work together, we welcome your suggestions and feedback. 

Business Model


Our primary business model is based on the bridging the partnerships between pharmaceutical/biotech sponsors and health care practitioners in academics and teaching hospitals for their R&D and Clinical Studies in developing effective therapeutics: Drugs, Devices and Vaccines.  Using best available technologies, this method provides a unique platform to fasten the innovation to a defined pharma market that is effective, unbiased, accurate, and time- and cost-effective.  

Our Services

  • Regulatory support
  • Drug & Device Establishment Licence
  • Drug & Device Identification Number Licence
  • ​IND/CTA maintenance
  • Clinical study/trial management
  • Electronic Real-time Data capturing 
  • Secure data management: validation, storage and archiving 
  • Scientific and Medical writing
  • R&D plans development
  • SOPs and protocols development
  • Licensing for drugs and therapeutics
  • ​Controlled Drug Substances 
  • ​Marketing: Market ResearchPost-market support