The Schedule in Drugs and Cosmetics Act that deals with the requirements and guidelines for clinical trials, import manufacture of new drugs is.
A. Schedule-O
B. Schedule-M
C. Schedule-F
D. Schedule-Y
Answer: Option D
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In the D & C act the schedule relating to GMP is
A. Schedule M
B. Schedule T
C. Schedule S
D. Schedule
MRP of scheduled formulations = Ceiling Price +
A. Retail Price
B. Local Taxes as Applicable
C. None
D. All of the above
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