Clinical Research Company

Full ServiceContract Research Organization

Clinical Research Company

ClinicalTRIALS SERVICES

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

BA /BE STUDIES

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

LABTESTING

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

Functional Service Providers

TEAM OF PROFESSIONAL

Strict adherence to frequently changing regulations

Pharmacologist

Cosmetics Personal Care & OTC products

Bio-analysts

PharmacovigilancePMS

  • Clinical Trials

  • Central Lab

  • BA/BE Studies

  • R & D Centre

ICBio - Contract Research Organization

ICBio CRO is a leading Contract Research Organization based in Bangalore, INDIA, offering clinical Trial services; phase I to phase IV, Bioequivalence, Bioavailability, Pharmacokinetic / Pharmacodynamic studies, Statistical Analysis and Data Management strictly adhering to ICH GCP guidelines. The company offers competitive and high quality clinical trial services to domestic and international pharmaceutical and Bio-Pharmaceutical companies.

Our facility is approved by Drug Controller General of India (DCGI), CDSCO, ISO 9001:2015, ISO 14001:2004, ISO / IEC 27001:2005, OHSAS 18001:2007, ISO 15189:2012 / NABL Accredited Clinical Laboratory, Inspected and approved by Ministry of Health-Kazakhstan and other relevant regulatory authority requirements.

ICBio CRO is specializes in conducting clinical research, Bioequivalence and Bioavailability studies. Our BA/BE facility is Fully Loaded Clinical unit with ICU Beds for conducting BA/BE studies with Access controlled area’s like Clinical Units / CPU, Bio analytical Laboratory, Volunteer screening, Volunteer Information centres, Central laboratory & Archives, Pharmacy. The ICBio has intensive care units, diagnostic and well-equipped laboratory and pharmacy spread over a floor area of 20,000 sq.ft,

Analytical laboratory is equipped with LC-MS/MS AB Sciex API 3200 & LC-MS/MS (Shimadzu 8040) instrument, other modern instruments & equipment’s.

The Studies are conducted as per the Guidance of ICH-GCP, declaration of Helsinki, Indian Council of Medical Research (ICMR) and Schedule Y, GLP and 21 CFR (part 11) guidance’s and also adhere to timely execution of projects within budget and accurate, reliable and comprehensive data by following applicable regulatory guidelines.

We are proud of our excellent track record and served a more than 100 satisfied customers. Meeting every timeline excellent quality. We have consistently exceeded our customers' expectations in terms of quality, speed and affordability.

We invite you to audit our facility.

Team ICBio CRO

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.



Departments
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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Biostatistics
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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