To enable supply to UK and other European markets
Kopran has announced that the United Kingdom, Medicines and Healthcare products Regulatory Agency (UKMHRA) has granted the Certificate of Compliance with principles and guidelines of Good Manufacturing Practice for the Finished Dosage Forms facility located at Savroli, Khalapur, Khopoli manufacturing general capsules and tablets.The approval for this facility shall enable the Company to supply Finished Dosage Forms to the UK and the European market for which necessary marketing tie-ups are being entered into.
The facility also has approvals from Regulatory Authorities of several countries all over the world including the Medicines Control Council, South Africa (MCC) and the Therapeutic Goods Administration, Australia (TGA).
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