The Medicines and Healthcare Products Regulatory Agency of the United Kingdom (UK-MHRA) has successfully concluded an inspection at Indoco Remedies’ sterile manufacturing facility (Plant II) at Verna, Goa. The inspection was held from September 16, 2019 to September 20, 2019 and resulted in 2 observations. Following this recent inspection, the sterile manufacturing site is expected to receive the EUGMP certification soon.
Indoco Remedies is engaged in the manufacturing and marketing of formulations (finished dosage forms) and active pharmaceutical ingredients (APIs) in India.