LCRA Services

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The core team of LCRA has vast experience of setting up CROs of international standards, managing clinical trials compliant with international regulatory guidelines.

With an experience of more than 2,000 biostudies, clinical trials, pharmacovigilance and clinical data management projects, the team has experience of successfully completing more than 40 regulatory audits including USFDA, EU, WHO, TGA Australia, ANVISA Brazil, MCC South Africa, MCC Zimbabwe and MoH Turkey.

The main objective of the Learning division at LCRA is to provide trained manpower to the clinical research, pharmaceutical and biotechnology industries.

The LCRA team constantly working towards upgrading clinical and bio-analytical competencies that are tuned to meet and satisfy customer requirements.


LCRA combines the highest levels of academic expertise with the latest in technology to effectively train and impart skills to students and professionals who intend to take up careers and specialize in the clinical research and pharmaceutical sciences domain.