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Our Clinical Research Project services include, but not limited to conducting site feasibility studies, ethics committee applications, undertaking site initiations, monitoring, and close-out visits, as well as overall project management, clinical data management services, pharmacovigilance, ICF translations, statistical analysis, and reporting as well as regulatory dossier submissions.

For complete information on our wide range of project support, download our e-brochure.

For inquiries/Requests, Please fill the form below and submit it.