IGMPI India

October 7, 2015

PAN Drugs receives warning letter from USFDA

MHRA issues recall notice of Lacri-Lube eye ointment

Another Import Ban for Polydrug Laboratories

Health Canada lifts its ban from two Apotex facilities in India

33 drugs were found to be of not of standard quality during Surprise inspection

Vivimed Labs successfully completes USFDA inspection of its manufacturing facility

October 7, 2015

PAN Drugs receives warning letter from USFDA

USFDA has recently issued a warning letter to PAN drugs Vadodara based plant due to significant deviations from good manufacturing practices.

MHRA issues recall notice of Lacri-Lube eye ointment

The Medicines and Healthcare Products Regulatory Agency (MHRA) has issued a recall notice to Allergen Limited. The recall notice relates to 5g and 3.5g pack sizes of

Another Import Ban for Polydrug Laboratories

USFDA (Food and Drug Administration) issues import ban for products manufactured by Polydrug Laboratories. It was issued on Sept. 11, 2015 for

Health Canada lifts its ban from two Apotex facilities in India

Health Canada has lifted its ban from Apotex two Indian facilities. Canada’s drug regulator reinspected the two plants in June and determined

33 drugs were found to be of not of standard quality during Surprise inspection

Recently Karnataka drug control department had conducted surprise inspections to pick up drug samples at random. The drug test labs have issued their result.

Vivimed Labs successfully completes USFDA inspection of its manufacturing facility

Vivimed Labs has recently successfully completed inspection of its API manufacturing facility in Spain. After the completion of inspection Vivimed said “the USFDA inspectors concluded

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GMP certification to be reviewed by Taiwan Ministry

It has been announced that the Ministry of Economic Affairs (MOEA) plans a review and evaluation of its regulations regarding Good Manufacturing Practice (GMP) certification. The Ministry aims at examining all GMP-labeled products within three months. This seems to be the result of the edible oils issue as the oils owned a certificate and yet were found to contain illegal additives.

As stated by the concerned authorities in the Ministry, there are plans to review the rule of GMP certification in within a period of one and half months. Also, all the 3682 GMP products would be examined in the next three months. These products include 129 oil products, 376 juice and soy sauce related products.

According to the legislators, the ministry may be blamed for the lax supervision of the private organizations that issue GMP certificates and are funded by the government. There have been demands to remove the concerned persons related to adulterated products. The ministry finds it necessary to address consumer doubts and hence the present step of reviewing GMp certification has been taken.