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2 min read | Updated on December 04, 2024, 08:58 IST
SUMMARY
Granules India shares tumbled on Tuesday as the company announced that the United States Food and Drug Administration (USFDA) has classified the inspection of the Gagillapur unit as ‘Official Action Indicated’ (OAI).
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The company further said that Granules’ growth trajectory remains robust and diversified.
An OAI classification from the USFDA means that regulatory and/or administrative actions are recommended for a particular/said unit.
Granules India was inspected between August 26 and September 6, 2024, and was given six observations.
However, the stock is expected to recover some lost ground as on Wednesday, the company shared a fresh update wherein it said that this classification (OAI) does not impact the ongoing manufacturing, distribution, or sale of existing products from the site.
However, it may impact the review of pending submissions from Gagillapur for approval of new products until the OAI status is resolved.
The company, in its filing, said, "Granules has undertaken a proactive, voluntary, and comprehensive remediation plan to address the six Form 483 observations raised by the USFDA. As part of this effort, we voluntarily paused manufacturing and dispatches in September to conduct a thorough risk assessment, ensuring no product contamination or patient safety concerns."
"Operations and dispatches have since resumed following this assurance. Our voluntary remediation plan includes robust corrective and preventive actions (CAPAs), oversight by an independent third party, continued product testing for risk assessment, and regular monthly progress updates to the USFDA. To date, over 80% of CAPAs have been completed, with the remainder on track for closure by March 2025. We are now seeking a meeting with the USFDA to present our progress and request a potential reinspection," the filing added.
The company further said that Granules’ growth trajectory remains robust and diversified, underscoring that the company's strategy is not solely dependent on new product approvals from the Gagillapur site.
"Key drivers include new launches from our GPI facility in the US, growth from large-volume products in the US and Europe, capacity addition, and commercialization of greenfield formulation facility at Genome Valley, value chain advancements in Europe, and our expanding oncology pipeline from Unit V. These initiatives ensure sustained performance as we work towards resolving the OAI status and reinforcing our commitment to compliance," the statement read.
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