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"3. PERMISSION The necessary drug manufacturing licenses as well as Central Excise Formalities will be undertaken and completed by CACHET. The necessary information and documentation required for the purpose will be provided by ALKEM. CACHET will keep necessary records as per FDA and GMP requirements and Excise Laws and documents to avail Modvat benefits.
6. SPECIFICATIONS Necessary specifications, manufacturing and assay methods for raw materials and finished product will be given by ALKEM. CACHET will ensure that adequate process controls and proper records for the same are maintained and that the finished product meets the specification laid down for the same.