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What to include

The more of this you provide up front, the more useful the reply will be.

• The product, molecule or excipient, with the grade or pharmacopoeial standard if you have it
• For excipients, what the material has to do in the formulation
• Quantity, and whether this is a trial, a one off or a recurring requirement
• The destination market, since this determines which certification is acceptable
• Any documentation your regulator or importer has already specified
• Your timeframe

Technical enquiries are answered by Dr. Qaria directly rather than by a sales desk.