ICBio CRO is a leading Contract Research Organization based in Bangalore, INDIA, offering Clinical Research services; Phase I – IV Clinical Trials and Bioavailability / Bioequivalence studies in Healthy volunteers as well as Patients to the Pharmaceuticals, Biotech, Nutraceuticals and Cosmetics Industries in India.
ICBio CRO is approved by Drug Controller General of India (DCGI), CDSCO. ISO 9001:2012, ISO 15189:2012 / NABL Accredited Clinical Laboratory, Inspected and approved by Ministry of Health-Kazakhstan and other relevant regulatory authority requirements.
ICBio has a well-designed, State of art infrastructure to conduct various activities with independent operational areas for Clinical Trials, BA/BE studies, Medical Writing, Clinical Data Management and spread over a floor area of 20,000 sq.ft,
Our BA/BE facility has 24 beds for conducting BA/BE studies with Access controlled area’s like Clinical Units / CPU, Bio analytical Laboratory, Volunteer screening, Volunteer Information centers, Central laboratory & Archives, Pharmacy. The ICBio has intensive care units, diagnostic and well-equipped laboratory and pharmacy.
All our services are conducted in strict adhere to ICH-GCP, 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 Client focused, flexible and also cost effective CRO in India; we focus on quality and add value services to our clients'. ICBio served a more than 30 satisfied customers. We have consistently exceeded our customers' expectations in terms of quality, speed and affordability.
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