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USFDA issues 6 observations for Cipla Goa plant

Ruchika SharmaWritten by Ruchika Sharma Published On 2022-08-27T16:11:46+05:30  |  Updated On 27 Aug 2022 10:41 AM GMT
USFDA issues 6 observations for Cipla Goa plant

Mumbai: Pharma major, Cipla has announced that the company has received six observations from the US Food and Drug Administration (USFDA) following the inspection conducted in August 2022 at its Goa plant.The company said the Goa plant recently underwent a United States Food and Drug Administration (USFDA) inspection from August 16 to 26, 2022.Earlier, the USFDA had inspected the...

Mumbai: Pharma major, Cipla has announced that the company has received six observations from the US Food and Drug Administration (USFDA) following the inspection conducted in August 2022 at its Goa plant.

The company said the Goa plant recently underwent a United States Food and Drug Administration (USFDA) inspection from August 16 to 26, 2022.

Earlier, the USFDA had inspected the company's Goa manufacturing facility in September 2019. A warning letter for the same was received by the company in February 2020.

Company further informed that on conclusion of the inspection, the company has now received 6 observations with some referencing to the observations made during the September 2019 inspection. There are no data integrity observations.

"The company will work closely with the US FDA and is committed to address these within the stipulated time, Company said in a filing with BSE.

Read also: Cipla EU to acquire additional 19.16 percent stake in Cipla Maroc

Cipla Limited is an Indian multinational pharmaceutical and biotechnology company, headquartered in Mumbai, India. The Company was founded by Khwaja Abdul Hamied in 1935 in Mumbai.

Cipla primarily develops medicines to treat respiratory, cardiovascular disease, arthritis, diabetes, weight control, depression, and other medical conditions.

Read also: Cipla gets CDSCO panel nod to study Rizatriptan Benzoate Orally Disintegrating Tablet



cipla cipla news USFDA goa facility USFDA inspection 
Source : with inputs
Ruchika Sharma
Ruchika Sharma

    M.Com

    Ruchika joined Medical Dialogue as an Desk Editor 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

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