ICBio Clinical Research is a full-service Contract Research Organization (CRO), based in Bangalore, INDIA, providing comprehensive, quality & integrated and an end to end clinical research solutions; Clinical Trials (Phase I-IV), BA / BE studies (Bioequivalence studies), Clinical Endpoint studies, provide quality clinical research solutions in India & across the world to its clients for studies ranging from PK studies in healthily volunteers to patient trials for generics and NCEs.
ICBio is Inspected and approved by Drug Controller General of India (DCGI) CDSCO India, ISP Chile, MOH Kazakhstan. NABL Accredited Central laboratory with integrated with LIMS. We serve to Pharmaceuticals, Cosmetics, Personal care, OTC Products, Medical Devices, and Nutraceuticals & Herbals companies. Our 32 bedded clinical facility with fully access-controlled state-of-art and UPS back-up. Up Coming with state-of-art 80 bedded II clinical facility.
ICBio conducted BA/BE studies for various regulatory agencies worldwide like FDA Philippines, Vietnam, Tanzania, MOH Kazakhstan, all CIS countries, and ISP Chile. We have been successfully doing many Clinical Studies for many Ayurveda, Herbal, Pharmaceutical, Nutraceuticals Dermatology Companies around the Globe. Our vision is to deliver enhanced CRO solutions on-time, we strive our best to meet the Highest Quality, cost-effective, data integrity, and Operational Excellence. We are grateful to our clients, who have shown faith in us to launch their products in the regulated, semi-regulated, and other markets
ICBio offer cost effective, result oriented studies for Bioequivalence studies, Clinical Trials, Bio analytical Services, PK / PD studies, Medical Writing, Biostatistics and Data Management, PSUR and Pharmacovigilance services to clients according to their requirements. We also provide Regulatory services like preparation of ACTD and CTD Dossier for export / product registration.
Last but not the least, we are a preferred cost-effective CRO for ROW markets; however we conduct studies in compliance to 21 CFR, GCP, and GLP; we have done studies for DCGI, CDSCO, FDA Philippines, DCEA Tanzania, MOH Vietnam, MOH Kazakhstan, and all CIS countries.
We also invite you to audit our facilities and look forward to experiencing our value-added services.
What We Do
BA/BE Studies are conducted at ICBio are in strict Compliance with International Regulatory Requirements, monitored by an independent quality assurance department.
Clinical trials are integral part of Drug Development. ICBio CRO offers end-to-end services for Phase II to IV clinical trials on small molecules, large molecules and medical devices.
The complexities and costs of clinical data management have shown a significant increase with cross-national, multi-centric trials and data collation from multiple sites. For Consistent...
ICBio being one of the best CRO in India provides regulatory services to facilitate all stages of drug development. We accomplish this by providing interdisciplinary strategy planning..
The success of a clinical development program depends on the proper documentation of research plans and results. ICBio offers a range of flexible Medical Writing services...
Our focus is to ensure the integrity of your data and organize your findings and conclusions into a clear and results-oriented presentation. Our bio statistics for clinical research..
Herbal and neutraceutical products have become increasingly popular in recent years and companies are looking for options to develop products most efficient,...
we will help you to develop and commercialize your cosmetic and skincare product, clinical evidence that your product is safe and effective can mean the difference between getting noticed and getting lost in the shuffle.