Emerging Markets Regulatory Tracker: India (Vol. 4 No. 68)
This article was originally published in PharmAsia News
India’s CDSCO has issued a notice on stability testing requirements for API exports to the EU that cuts the timeframe from one year to six months.
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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.