New Delhi, April 18: The Indian Pharmacopoeia Commission (IPC), in collaboration with the Council of Scientific and Industrial Research (CSIR), organized a scientific conference and interactive session on the Indian Pharmacopoeia (IP) 2026 at the CSIR-Indian Institute of Integrative Medicine (CSIR-IIIM) in Jammu on April 17, 2026.
Experts from regulatory bodies, academia, and the pharmaceutical sector gathered to discuss significant developments in pharmacopoeial standards and their role in ensuring the quality, safety, and efficacy of medicines.
During the inaugural session, senior officials and specialists emphasized the importance of strengthening pharmacopoeial standards in line with evolving scientific and regulatory requirements. The discussions highlighted the role of the Indian Pharmacopoeia as a crucial tool for maintaining uniform standards for medicines across the country.
Technical sessions focused on the latest updates in the Indian Pharmacopoeia (IP) 2026, including the development and revision of regulations, strengthening impurity standards, and adopting modern analytical approaches. Topics such as regulatory perspectives, standardization of herbal medicines, and enhancing microbiological and blood-related standards were also included. This reflects a comprehensive approach towards improving drug quality systems.
The interactive session provided a platform for stakeholders to exchange views on the implementation aspects of IP 2026, industry readiness, and the need for continuous alignment with global standards. Participants highlighted the importance of collaboration among regulators, industry, and scientific institutions for the effective adoption of the latest standards.
The conference reiterated the commitment of the Indian Pharmacopoeia Commission (IPC) to continuously advance pharmacopoeial standards through scientific progress and stakeholder engagement. This will contribute to strengthening public health safety measures in the country.
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