Noida, India·50-200 employees
IR Innovate Research is a regulatory compliant full-service Contract Research Organization With a strategic presence across the globe, We specialize in providing End-to-End…
ProClin Research pvt. ltd.
CROPrivate Company
Hyderabad, India
2019
Founded10-50
Employees121
Trials supported93,000
Patients enrolledAbout ProClin Research pvt. ltd.
ProClin Research is a specialist clinical research organization (CRO) providing services to Pharma Companies/Sponsor. ProClin provides the full range of clinical research, Data Management and Training. ProClin provides entire range of services and facilities necessary for the fast-track, high-quality development of medical devices, pharmaceutical products and combinations in phase I to IV clinical studies, registries, post- marketing studies and investigator sponsored studies. All processes are in compliance with Good Clinical Practice (GCP), guidelines of the European Medicines Agency (EMA), Food and Drug Administration (FDA) and according to International Conference on Harmonization (ICH) and ISO standards. Currently we are managing various studies on Diagnostics, Nutraceuticals and New drugs for different regulatory submissions, our expert medical advisors on various therapeutic areas help in conduct and designing of the study effectively. We are working in various therapeutic areas such as oncology, ophthalmology, cardiovascular, gastroenterology, sports nutrition, immunology, respiratory including COVID-19, cosmetics and diagnostics. Our entire studies are guided by highly experienced medical advisors and are being supplemented by our core operations team.
Services
Protocol and Study DesignPatient Recruitment and EngagementStartup Services and Site ManagementVendor Selection and Strategic OutsourcingData Sources and Data ManagementClinical Study ReportClinical Trials Support SoftwareStaffing and WorkforceRegulatory Services, Study Report, AE ManagementSite Management
Therapeutic areas
Experience & capabilities
Trial phases:Phase 1Phase 2Phase 3Phase 4
Products:Medical DevicesDiagnosticsTherapeutic productsVaccines
Trial geography:GlobalEuropeSoutheast AsiaSouth AsiaEast AsiaNorth America
Compliance:Audited by FDAGDPR compliant21 CFR Part 11 compliant
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