HYDERABAD, India, Oct. 28, 2024[1], announced that it has received Establishment Inspection Reports (EIR) from the US Food and Drug Administration (USFDA) for its R&D (Unit II, Hyderabad), and Manufacturing (Unit IV, Bidar) sites in India.
The General Good Manufacturing Practices (GMP) audit was conducted at the integrated R&D campus (Unit II) in April 2024, while the pre-approval inspection (PAI) & General GMP audit was conducted at the Manufacturing facility (Unit IV) in Bidar in June 2024.
Making the announcement, Krishna Kanumuri, CEO & Managing Director of Sai Life Sciences, said, "These audit outcomes reflect Sai Life Sciences' commitment to maintaining the highest standards of quality and compliance across its R&D and manufacturing facilities. It demonstrates the company's robust quality systems and its readiness to support the supply of high-quality pharmaceutical products to global markets."
[1] Among listed Indian peers in terms of revenue CAGR as well as EBITDA CAGR over FY22-24.
About Sai Life Sciences:
Sai Life Sciences is the fastest-growing contract research, development, and manufacturing organisation
A photo accompanying this announcement is available at https://www.globenewswire.com/NewsRoom/AttachmentNg/8a591e96-ed90-416a-b690-4cf120b64d12
