Clinical Development

The Clinical Development and Medical Affairs (CDMA) team at Biocon Biologics is pivotal to the success of our biosimilar strategy, driving the execution of high-quality clinical trials. The key arms of the clinical development function— Clinical Sciences, Biostatistics, Clinical Operations, Pharmacovigilance, Medical Communication, Quality & Compliance, and Global Medical Affairs — work in tandem to ensure that our biosimilars meet rigorous scientific and regulatory standards, to reach the market in a timely and cost-effective manner.

Clinical Development

Global Medical Affairs

The Global Medical Affairs team bridges the gap between Biocon Biologics and the healthcare community by delivering accurate, up-to-date scientific data on our biosimilars.

The team is responsible for educating healthcare professionals (HCPs) on the potential of biosimilars to promote equitable care and sustainability, playing a pivotal role in advancing the scientific and clinical understanding of our biosimilars and biologics portfolio. In addition to supporting the development of clinical guidelines in close collaboration with regulatory bodies, it leads key medical education initiatives, including webinars and scientific conferences, to foster knowledge exchange and drive innovation. 

Through active engagement with Key Opinion Leaders (KOLs) and stakeholders, Global Medical Affairs facilitates collaboration, shares clinical insights, and drives confidence in the adoption of biosimilars, for improved patient care.

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Regulatory Sciences

This division plays a critical role in supporting the successful development and global commercialization of biosimilars. The team’s active participation...
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R&D Pipeline

Our robust R&D pipeline is the cornerstone of our growth strategy. A firm belief in ‘our pipeline is our lifeline’...
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