EMA clears Ranbaxy

June 10, 2014

ALTHOUGH some Good Manufacturing Process (GMP) deficiencies were found at the Ranbaxy Toansa site in India, the European Union has assessed that there has been no resultant risk to public health. The EMA and FDA investigations followed shortfalls in quality controls at the Toansa facility which resulted in bans for products exported from there (PD 24 Jan 14). European regulators also considered the corrective measures put in place and were satisfied they were sufficient to ensure GMPcompliant manufacture of products at the site.

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Pharmacy Daily | EMA clears Ranbaxy

EMA clears Ranbaxy

Other recent headlines

Brooke Shelly wins big

PSA’s credentialed members package

Putting patients at the centre

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES