Medclinica Private Limited

In their own words

MedClinica is a global CRO. MedClinica offers Clinical Trial Services like Medical Writing, Clinical Operations, Data Management, Biostatistics & SAS programming, Pharmacovigilance, Regulatory, Project Management, Quality Assurance & Auditing for Phase I to Phase IV Studies for Pharmaceutical, Biotech, Medical Devices, and Nutraceutical companies. MedClinica also supports, Post Marketing/Observations, Late Phase, Registries, Cohort, IIT, Rx Based, and Retrospective Studies. MedClinica conducts the trials under strict adherence to ICH-GCP, EMA, and USFDA, complies with local, national, and international regulations, and is dedicated to high-level protocol compliance with proactive communication to all relevant stakeholders. MedClinica team members have a proven track record of rendering high-quality services to Pharmaceutical, Biotech, Medical Devices, and Nutraceutical companies. MedClinica Teams are highly qualified and experienced in conducting multicentric global clinical trials in various therapeutic areas, for end-to-end Clinical Trials in Phase I to Phase IV, & Late Phase trial services. MedClinica team consists of experienced pharmacologists, Medicos, Health Care Professionals, Project Managers, Data Managers, CRAs, Trial programmers, Biostat and SAS experts, highly experienced medical and scientific writing teams, and QA & Regulatory Specialists. MedClinica utilizes its resources based in US and EU- Subject Matter Experts (SME) to provide direct project oversight. 1. MEDCLINICA SERVICES MedClinica is a global clinical trial service provider providing the following Clinical Trial services:  Medical Writing  Clinical Operations  Project Management  Data Management  Biostatistics & SAS programming  Pharmacovigilance  Regulatory  Central SMO  Medical Devices

Written by the company on its public Startup India profile. Not verified by us.