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, a Independent Contract Research Organization (CRO), based in Bangalore (INDIA); providing quality clinical research solutions in India & across the world to its clients for studies like PK studies on healthily volunteers, patient trials for generics, We can support you with our experience, expertise and valued-added service from IC Bio.

ICBio providing integrated clinical offerings in Early Phase Clinical Trials, Late Phase Clinical Trials (Phase II-IV), Bioequivalence studies (BA/BE studies), Clinical Endpoint Trials, Bio analytical, Dermatology, Respiratory, Allergy and Personal Healthcare services.

ICBio also offers clinical safety and efficacy studies for Nutraeuticals, Herbals, Cosmetics and OTC Product companies.

  • Our facility is approved by Drug Controller General of India (DCGI),
    DSIR recognized in-house R&D,
    Frequently audited by  MoH, Kazakhstan (5 times),
    NABL accredited Clinical Laboratory with integrated with LIMS.
  • 10,000 volunteer data base and VIMS software for volunteer management
  • 24 bedded facility with fully access-controlled state-of-art and UPS back-up
  • Exclusive strategies in place to strive for 100% subject turn-out to cover the complete sampling schedule
  • Bio analytical laboratory is equipped with LC-MS/MS 8040, LC-MS/MS 8050 (Shimadzu),
    PerkinElmer's NexION 1000 ICP-MS along with other modern instruments & equipment’s and validated methods for 125 molecules. Team can do MD & MV within 2-3 weeks.
  • Completion of BE study within 3-4 months from initiation to completion
  • Network with 150 hospitals and expertise in 18 TAs to conduct late phase clinical trials;Phase II to IV

We strive our best to meet the Highest Quality, Economic Budgets, Speedy Timelines and Operational Excellence.

Please go through the attachment for details on our capabilities & regulatory approvals.

We are driven 24x7 by the passion that ignites the inspiration every day and our inspiration comes from our clients. We are grateful to our clients, who have shown faith in us to launch their products in the regulated, semi-regulated and other markets.

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 CIS countries, Philippines, Tanzania, Vietnam, Ukraine etc.

We invite you to audit our facilities and look forward to experience our value-added services.

Team ICBio

Business Enquiry Form
Why to choose ICBio
  • Approved by Drug Controller General of India (DCGI)
  • 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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