At Rayfacts CRS we are determined to conduct original research work in Real World scenario using specific needs and with following objectives:

  • The evaluation of the clinical effectiveness and safety based on real-world data.
  • Exploring real-world data for potential patterns of Therapies/ Drugs
  • Support better patient outcomes.

We had been able to attain the above objectives by generating data through the following projects:

  • Late Phase studies: Post Marketing Surveillance, Prospective/ Retrospective studies, Disease/ Patient registries, Longitudinal studies, Investigator Initiative studies etc.
  • Regulatory writing including Original articles, systemic reviews, meta analysis, case studies with publications , review articles etc.
  • Conducting Markets research activities including both Qualitative and Quantitative researches including publications.
  • Developing Consensus statement based on Delphi recommendations with Publications.

Following are the best industry practices are adhered at Rayfacts during execution of projects:

  1. Rigorous feasibility and site evaluation
  2. Transparent study planning and execution
  3. Continuous oversight of patient recruitment and engagement
  4. Exceptional data quality and integrity as per international standards
  5. Regular monitoring and quality assurance reviews
  6. Structured study closure with audit readiness

We leverage a strong network of investigators, sites, SMO's and IEC/IRB's and healthcare providers across therapeutic areas ensuring robust study participation and timely data capture. Our reach has enabled us to build up a strong network of more than 145 hospitals and 1200 sites

Our leadership team brings 20+ years of experience in managing clinical studies across therapeutic areas, delivering high-quality data and patient outcomes.

We have a working experience of 37 Late Phase Studies and 20+ scientific and regulatory writing projects with an internal team size of 25 members

We adhere to strict compliances such as NDCT Rules -2019, ICH-GCP, local regulations, EC approvals, CTRI and DCGI guidelines, and Global data privacy laws (GDPR, HIPAA). ISO 9001:2015, ISO 27001