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  • USFDA successfully...

USFDA successfully completes inspection at Solara Ambernath facility

Written By : Ruchika Sharma |Medically Reviewed By : Dr. Kamal Kant Kohli Published On 2025-05-12T11:30:11+05:30  |  Updated On 12 May 2025 11:30 AM IST
USFDA successfully completes inspection at Solara Ambernath facility
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Chennai: Solara Active Pharma Sciences Limited, an Active Pharmaceutical Ingredient provider, has announced that its multi-product manufacturing facility at Ambernath, Maharashtra has successfully completed the inspection carried out by the US Food and Drug Administration (US FDA).

The inspection established that the site is in an “Acceptable State of Compliance” with Zero Form 483 inspectional observations from US FDA.
The Agency with their designated investigator inspected the facility from 5 th to 9 th May 2025.
Commenting on the Inspection Outcome, Sandeep Rao, MD & CEO said, “We are very happy with the successful inspection outcome of our Ambernath API site with Zero 483 inspectional observations. This is the third (3rd) consecutive successful inspection outcome, with Zero 483 inspectional observations, across the Solara network of manufacturing facilities. The inspection outcome demonstrates our commitment to regulatory excellence at our global manufacturing sites and relentless focus on world-class quality and compliance, which remains a key pillar of our growth strategy. We stay committed to exhibit the highest level of compliance and constant focus on world-class quality with the validated quality systems established across Solara’s manufacturing network.”

An FDA Form 483 is issued to firm management at the conclusion of an inspection when an investigator(s) has observed any conditions that in their judgment may constitute violations of the Food Drug and Cosmetic (FD&C) Act and related Acts.

The Ambernath multi-product API manufacturing facility was established in the year 2004 and is equipped with appropriate infrastructure to include several independent production blocks and related packaging sections. This site is inspected by various Regulatory Authorities including US FDA, EDQM, WHO, PMDA, and KFDA.
Solara Active Pharma Sciences Ltd is a global API manufacturer supported by state-of-the-art R&D and manufacturing facilities. With 6 manufacturing facilities and an R&D Centre, Solara offers a basket of diversified Commercial APIs and Contract manufacturing services. Its API facilities are approved by various international regulatory agencies including the USFDA, EDQM, MFDS, WHO, PMDA etc.
Read also: USFDA concludes inspection at Solara Active Pharma Sciences Vizag facility with Zero 483 inspectional observations
solara activa pharma sciencesUSFDAUSFDA inspection
Ruchika Sharma
Ruchika Sharma

    Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751

    Dr. Kamal Kant Kohli
    Dr. Kamal Kant Kohli

    Dr Kamal Kant Kohli-MBBS, DTCD- a chest specialist with more than 30 years of practice and a flair for writing clinical articles, Dr Kamal Kant Kohli joined Medical Dialogues as a Chief Editor of Medical News. Besides writing articles, as an editor, he proofreads and verifies all the medical content published on Medical Dialogues including those coming from journals, studies,medical conferences,guidelines etc. Email: drkohli@medicaldialogues.in. Contact no. 011-43720751

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