Emerging Markets Regulatory Tracker: China GSPs, Indian BE Testing
This article was originally published in PharmAsia News
China has issued new Good Supply Practice regulations for medical devices, while India is changing the format of requests for bioequivalence studies for drugs to be exported.
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India’s health ministry has laid out basic steps towards an overhaul of drug regulation at the local level, identifying a number of areas of concern.
China has released the results of back on proposed standards for the accreditation of clinical trial committees, investigators and sites.
China has finalized revised rules for the classification of medical devices, which will come into effect from the start of next year.