ETHOS CLINICAL RESEARCH
A CUSTOM OF INNOVATION IN CLINICAL RESEARCH
- Includes preparation and submission of clinical trial applications to regulatory authorities.
- Includes preparation of Ethics Committee documentation like SOP preparation for
Submission and Approval to (CDSCO) Central Drugs Standard Control Organisation.
- Includes the protocol writing for Clinical trials to be started in India.
- We have a Quality Team trained in GCP and CDSCO guidelines of 2019 and we also provide
the same training as per the requirements with certification.
- We have senior regulatory specialists on hand, dedicated to managing the ethics and
regulatory approvals to ensure an efficient and timely start of your studies. Our experience
in regulatory affairs covers the competent authorities in the Indian and in Central and
Eastern European countries (where this offering from Stridden is available either as a stand-
alone service or as part of our site management services).
