Conduct Bioequivalence Study: CDSCO panel tells Abbott India on Dydrogesterone MR Tablets
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New Delhi: Responding to the proposal for manufacturing and marketing synthetic progesterone, Dydrogesterone Modified-release (MR) Tablets presented by Abbott India, the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has recommended the firm to conduct the bioequivalence (BE) study as per the protocol and submit the report along with the clinical trial protocol.
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