Indian Regulators Reviewing CDSCO Processes for Reform

The Indian Drugs Controller General’s office has launched a new task force to review processes and procedures currently in place at the Central Drugs Standards Control Organization (CDSCO) in order to boost efficiencies in how medical devices and drugs are reviewed and approved for sale in the country.

CDSCO medical device registration processes under review in IndiaThe task force includes former regional CDSCO officials as well as industry representatives, and is charged with recommending shorter, more user-friendly processes, procedures and forms. The task force will have two months to complete its review, and will then submit recommendations to the Drugs Controller General.

Any specific recommendations for medical device registration and approval processes in India will be reported and analyzed following conclusion of the task force’s work.

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