India Pharma Outlook Team | Tuesday, 21 April 2026
Indian oncology medicine manufacturers are witnessing a clear disconnect between rapid scientific innovation — including targeted therapies, biosimilars, next-generation sequencing (NGS), minimal residual disease assays, and immuno-oncology treatments — and their on-ground implementation in clinical settings, especially in resource-constrained environments.
This gap threatens to limit the benefits of precision medicine for the vast majority of cancer patients in India, where diagnostic access, referral pathways, and affordability remain uneven.
Dr Shashank Srinivasan, Medical Affairs Director – Oncology Business Unit, AstraZeneca Pharma India, emphasised the shift brought by precision medicine: “Advances in precision medicine, cancer care in India has undergone a major shift. It is changing how the disease is understood and managed. This has opened doors to early intervention and personalised care. The challenge now is to ensure that these benefits are felt consistently in everyday practice.”
He further noted that bridging these barriers “requires a multidisciplinary, data-enabled, and patient-centred approach with disciplined execution across the care continuum.”
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Highlights:
Industry experts advocate several practical measures:
Dr Srinivasan added that expanding early detection, improving diagnostic reach, and standardising evidence-based care pathways are “critical steps to address inequities.”
The lessons from oncology extend to other high-burden non-communicable diseases such as cardiovascular, renal, metabolic, and respiratory conditions, where similar delays in diagnosis and fragmented pathways undermine patient outcomes.
In India, bridging science and practice is described as being “less about isolated breakthroughs and more about disciplined implementation.” Operationalising innovation demands focus on diagnostics access and quality, pathway standardisation, and effective navigation systems.
Without concerted action, the promise of transformative therapies risks remaining confined to select urban centres and clinical trials, rather than delivering measurable benefits to the wider population affected by cancer.
Manufacturers stress that when diagnostics, education, data partnerships, and coordinated care come together, scientific progress can translate into equitable and improved patient outcomes across the country.
Stakeholders expect intensified discussions in the coming months involving regulators, clinicians, medical associations, and patient groups to drive policy tweaks, capacity building, and faster integration of innovations into routine practice.