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Slide 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. Click here for more on Biometrics