Clinical Research Company

Full ServiceContract Research Organization

Clinical Research Company


ICBio provides Clinical Trial Services for pharmaceutical and biotechnology product development from phase II to phase IV for all multinational pharmaceutical companies./p>

Clinical Research Company


Bioavailability and Bioequivalence studies at ICBio is facilitated in a state-of-the-art

Functional Service Providers

Your Contract Research Organization inINDIA

Clinical Research Company

Medical writing Clinical Data management

Functional Service Providers


ICBio leading Central labs provides effective Lab Data management and high quality lab data within required timelines.

Functional Service Providers


Strict adherence to frequently changing regulations


Cosmetics Personal Care & OTC products



  • Clinical Trials

  • Central Lab

  • BA/BE Studies

  • R & D Centre

ICBio - Contract Research Organization

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.

ICBio Team

Business Enquiry Form
Why to choose ICBio
  • Approved by Drug Controller General of India (DCGI)
  • Approved by ISP Chile
  • Approved by Ministry of Health – Kazakhstan
  • NABL Accredited Clinical Laboratory
  • DSIR Approved R & D centre, Govt. of India
  • Certifications ; ISO 9001:2015, ISO 15189: 2012
  • ISO 14001:2015, ISO / IEC 27001:2013, OHSAS 18001:2007
  • Flexible working hours for global clients
  • Wide Pan India network of hospitals and Investigators- 150 sites in 17 different cities
  • Dedicated Project Management Team for each client
  • Diverse patient population database

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 & Nutraceutical Trials

    Herbal and neutraceutical products have become increasingly popular in recent years and companies are looking for options to develop products most efficient,...

  • Cosmetics, Personal Care & OTC products

    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.

Quality Assurance
Quality management provides quality systems which in turn guarantee good quality data in each clinical trial. Quality systems implemented at ICBIO and managed by Quality Management ensure the quality, integrity, and accuracy of data for each clinical study undertaken at ICBIO.

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Clinical Development
Clinical Operations team conducts Phases II-IV clinical trials for pharmaceutical and biotech companies, maintaining the highest standards of ethics, quality and confidentiality. A team of well-trained professionals, experience in project management in various therapeutic areas.

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Bio Analytical
ICBio management & operations team brings in considerable experience in conducting BA/BE studies on healthy as well as patient population with various dosage forms including injectables like IM/IV/SC, oral dosage forms like solid formulations (Modified Release preparations), liquid formulations, topical preparations and inhalations. The BA/BE studies conducted at ICBio are fully GCP compliant.

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Project Management
ICBIO's project management group stands out from other CROs in an industry where hard deliverables and quality of enrollment are everything. ICBIO project managers throughout the globe are obsessive about on-time project delivery from day one.

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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 and statistical programming services include pre-analysis, analysis and post-analysis.

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