When it comes to regulatory services, majority of CRO’s in India offer them in every stage of the Phase I – IV studies.

1. Importance of advanced Regulatory Services in CRO’s in India
When it comes to regulatory services, majority of CRO’s in India offer them in every stage of the Phase I – IV
studies. The same is also provided in various levels of drug development and is attained by providing
interdisciplinary planning to have the best regulatory method for regulatory authorizations.
CRO’s and Regulatory Services
There are several CRO’s that use the expertise of the expert medical technicians and then apply this knowledge to
multiple clinical assignments. There are also expert groups who are capable to managing a diverse range of
regulatory services and assist certain sponsors to cater to exigent timelines. Furthermore, CRO’s assists the
sponsors to get regulatory approvals because of their experience and understanding in Indian clinical research
policies.
India has flourished as the hub for medical tourism, clinical trials and other medical researches that are being
carried on by multinational pharmaceutical organizations. The chief reason for this is advanced healthcare options,
high-end equipments, quality and effective diagnosis and a team of expert healthcare professionals. Furthermore,
keeping in mind the population size of the company most people use English and are fluent.
The Modern Day Regulatory Services
Renowned CRO’s in India, have regulatory services and QA that comprise important elements of the service
portfolio being offered to people. There is a dedicated group for regulatory and audit compliance that are usually
backed up by the know-how of local regulatory processes and are an apt liaison with the multiple regulatory
agencies that guarantees efficiency in the clinical trial approval process.
Let us have a look at the selected regulatory services offered by the CRO’s are listed below-
 Compilation of the clinical trial application
 Obtaining approvals for conduct of clinical trials
 Procurement of drug import licenses
 Renewal of Import License
 Formulation of regulatory strategies
 Submission of Clinical Safety Report (CSR)
 Submission and follow-up of the application
 Safety Reporting
 Procurement of NOC for export of biological samples
 Tracking of applications and approvals
 Response to regulatory agency queries
Along with these regulatory services CRO’s also provide a clinical laboratory that helps in medical researches and
studies and is helpful for drug development and disease treatment.
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