Production of active pharmaceutical ingredients (APIs) at the API Industrial Park in Gazaria of Munshiganj will begin next month, with ACME Laboratories set to commission its manufacturing unit despite the lack of gas supply.
The High Court today directed the Directorate General of Drug Administration (DGDA) to give Tk 15 lakh as compensation to each of the families of the 104 children, who died after taking toxic paracetamol syrup in 1991 and 2009.
The pharmaceuticals industry is gearing up to expand as 19 companies have got the go-ahead in the last one year to set up facilities at a combined investment of around Tk 654.82 crore.
The Directorate General of Drug Administration (DGDA) has launched six international standard mini-labs in as many districts to enhance its capacity to check sale of fake medicines.
High Court summons Health Secretary Sirajul Haque Khan to appear before it on August 23 to explain why action was not taken against two officials of the drug administration.
We are informed by the Directorate General of Drug Administration that some 153 sub-standard drugs have been detected, of which, 43 had already been marketed and awaiting registration.
The drug administration will take legal actions against the pharmaceutical companies who did not withdraw three types of drugs, banned by the government recently, from the market.
Production of active pharmaceutical ingredients (APIs) at the API Industrial Park in Gazaria of Munshiganj will begin next month, with ACME Laboratories set to commission its manufacturing unit despite the lack of gas supply.
The High Court today directed the Directorate General of Drug Administration (DGDA) to give Tk 15 lakh as compensation to each of the families of the 104 children, who died after taking toxic paracetamol syrup in 1991 and 2009.
The pharmaceuticals industry is gearing up to expand as 19 companies have got the go-ahead in the last one year to set up facilities at a combined investment of around Tk 654.82 crore.
The Directorate General of Drug Administration (DGDA) has launched six international standard mini-labs in as many districts to enhance its capacity to check sale of fake medicines.
High Court summons Health Secretary Sirajul Haque Khan to appear before it on August 23 to explain why action was not taken against two officials of the drug administration.
We are informed by the Directorate General of Drug Administration that some 153 sub-standard drugs have been detected, of which, 43 had already been marketed and awaiting registration.
The drug administration will take legal actions against the pharmaceutical companies who did not withdraw three types of drugs, banned by the government recently, from the market.
