J.B. Chemicals & Pharmaceuticals Limited (JBCPL) has announce receipt of European GMP Approval for its formulation facilities in Panoli, Gujarat, India from Medicines Authority of Malta.
The inspection is outcome of a successful cGMP inspection carried out in September/October 2017.
Addition of other dosage form like Capsules, Liquids and Semi Solids will open the door of EU as well as PIC/S market for these formulations manufactured at Company’s Stateof-the-Art manufacturing facilities situated at Panoli.
The Company also intends to explore possibility of contract manufacture these formulations for EU market to leverage the approval.
JBCPL has world class Lozenges manufacturing facility in Daman, India, which also has cGMP accredited by EU Authorities in the year 2017. Thus, Company’s all formulations manufacturing facilities (non-sterile) enjoy EU approval.