Imported Products Allopathic – Guidelines Allopathic Products Application Forms Guidelines Guidelines For The Registration Of Allopathic Products Guideline on Variations FDA Reliance Guideline on Regulatory Decision Making Guideline on Donation of Drugs Guideline on Conducting Bioequivalence Studies Guidelines on Parallel Importation of Medicinal Products Guidelines on Registration of Allopathic Drugs Guidelines on Registration of Allopathic Drugs-Quality Guidelines on Emergency Use Authorization of Medical Products Guideline on FDA Public Assessment Report Guideline on Labelling of Drugs Guidelines on Naming of Medicinal Products Guidelines on Registration of Orphan Drugs Guideline on Registration of Allopathic Medicines Considered for Small Scale Manufacture Guidelines on Stability Testing of Active Pharmaceutical Ingredients and Finished Pharmaceutical Products Guideline on Registration of UK Generics Guideline for Importation of Drugs Guideline on the Registration of Medicinal Products Classified for Fast Track Processing Guideline on the Withdrawal, Cancellation or Suspension of Marketing Authorization of Drugs Process Flow and Timelines for Medicinal Product (Fast Tack) Registration(1) Process Flow and Timelines for Medicinal Product Variation Process Flow and Timelines for Medicinal Product Registration Process Flow and Timelines for Medicinal Product Re-Registration
