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
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.