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Regulatory Services: DMF Filing

If you are a supplier of drug product components, you are usually required to submit Drug Master Files (DMF) to regulatory authorities, to permit them to review specific product information (concerning the Chemistry, Manufacturing and Controls ), in support of your buyer’s submission. We can help you in preparing and filing Drug Master Files (DMF) in United States, Europe, China, Canada, Australia, Japan, and other countries around the world.
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