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Clinical Research

Inherent advantages such as low costs, access to a vast patient population and a large base of qualified personnel has made India an attractive destination for clinical research outsourcing (CRO). India's clinical research market, valued at $75 million currently, is set to increase to $500 million by 2010.

TransAsia Labs Pvt. Ltd. has built best practices in laboratory medicine and has clinical trial capabilities supporting doctoral & post-doctoral research studies, contract research organizations and/or Pharma companies. We have built capabilities to support CRO’s undertaking stage3 clinical trials, including supporting them on the data management and software systems to facilitate reporting compliance to CRO requirements. We have continuing interests in the Clinical research space and are keen to support CRO’s looking for reliable investigative outcomes in their trial along with systems capability to provide electronic data management in flexible formats.

At TransAsia Labs Pvt. Ltd., we adhere to ICH GCP standards, thus making our laboratory a destination for testing required by clinical trials and projects. If your project requires blood investigation for a specific test, we can assist you to plan and execute the research process.

TransAsia Labs Pvt. committed to providing accurate and timely laboratory testing services for the research community. We recognize that each clinical trial is unique and strive to customise services for each trial.

Researchers must obtain appropriate institutional approval and have proposals approved by the appropriate scientific and ethics review committee prior to starting each study involving clinical data obtained through TransAsia Labs Pvt. Ltd.

For further information please contact at +91 9906091412 or e-mail at

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