Market Place
Divi's Laboratories — an Indian active pharmaceutical ingredient (API) manufacturer and until recently the darling of the Indian bourses — received another setback this week.
The US Food and Drug Administration (FDA) placed its Unit
II, located in Visakhapatnam, on its import alert list for “refusing FDA foreign establishment inspection”
as also for “not meeting drug GMPs” (good manufacturing practices).
According to the FDA website “the refusal to permit inspection of a foreign facility or provide reasonable access to FDA’s inspectional personnel, combined with other evidence, provides an appearance that the firm’s products are manufactured, processed, or packed under insanitary conditions.” The firm is considered to have refused the FDA inspection.
This news comes as a surprise, as it adds an additional dimension to the problems that the FDA encountered at Divi’s facilities.
PharmaCompass
had
previously shared news that Health Canada had placed the company on its inspection tracker after data integrity and general GMP observations were reported by its “regulatory partner(s)”.
According to
media reports, the firm was inspected by the US FDA from November 29 to
December 6, 2016, and the regulators had issued an 18-page long Form 483 with five observations.
Second Divi’s group firm to refuse inspection
The news comes a few months after its affiliate – Divi’s Pharmaceutical Private Ltd was placed on FDA’s Import Alert List for refusing an inspection by the US
FDA.
The two
facilities of Divi’s Pharmaceutical that were placed on the FDA’s Red List were Divi Towers in Hyderabad, and a facility in Medak district, Telangana. Divi Towers is also the corporate headquarters of Divi’s Laboratories.
Divi’s Laboratories’ Unit-II is a major producer of APIs and a key supplier to leading companies around the world. The FDA has excluded some intermediates and the following APIs from the import alerts – Levetiracetam, Gabapentin, Lamotrigine, Capecitabine, Naproxen sodium , Raltegravir potassium and Atovaquone.
The exemptions did not help as far as the stock market was concerned. Divi’s stock price, which has already been under significant pressure after news of the inspection initially broke out in December, tanked another 20 percent on Tuesday.
Our view
While the details are yet to emerge on the exact nature of problems which the US FDA inspectors uncovered and encountered at Divi’s Laboratories Unit II, it is clear that Divi’s has a long road ahead insofar as regulatory compliance is concerned.
Impressions: 3526
https://www.pharmacompass.com/radio-compass-blog/divi-s-labs-on-fda-s-import-alert-list-but-did-it-refuse-an-inspection
#PharmaFlow by PHARMACOMPASS
23 Mar 2017
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