Shilpa Medicare Ltd's finished dosage form manufacturing facility, Unit IV, situated at Pharma SEZ, Jadcherla, Telangana state has successfully closed-out a GMP Inspection from TGA, Australia as per communication received on 17th October 2023.

The facility is involved in manufacturing, packaging, labelling, testing and release of finished dosage forms (sterile injections and non-sterile oral solids) for the treatment of various forms of cancer and adjuvant therapy.

This inspection is the fourth major regulatory inspection (after Russia, Canada and Brazil), cleared by this site in the past two years.

The successful closure of this inspection will allow the company to register and market its products in Australia and other rest of world markets which recognize Australian GMP.

The company remains committed to maintain the GMP status and quality standards as per the expectations and standards of Global Regulatory Authorities.