VCRO was established in 1997, aiming to offer ICH standard clinical research service in Asia. We have performed over 420 various projects in more than 41 therapeutic areas, moreover, all conducted commissions were accepted by TFDA, and all inspections from global clients were passed as well. We provide a full range service solution from IND to NDA, including bioanalysis, clinical trial planning and conduct, US FDA IND filing, and E-Tools. Through our professional, experienced, and trustworthy team, VCRO is confident in providing customized clinical service to fulfill our clients’ blueprint.
- VCRO has 100% TFDA approval record for more than 70 times of GCP inspections.
- VCRO has been granted as the best CRO in 2004 and 2007 by the National Science and Technology Program (NSTP).
- VCRO’s BioLab is accredited OECD GLP, TFDA GLP, and ISO 17025 certificates. Our bioanalytical data was accepted by the US FDA as well.
- VCRO launched a clinical trial information system (CTIS) in 2008, an EDC system integrated with clinical research knowledge management.
- VCRO launched Interactive Voice Response System (IVRS) in 2007 and Interactive Web Response System (IWRS) in 2011, which increased clinical study efficiency and applied in many global trials.
- Clinical Operations
- Regulatory Affairs
- Medical Writing & Consulting
- Biometrics and Data Management
- Bio-analytical Laboratory