(( Circular No. 011/DAR/2016 NDA drug register for December 2016 This is to inform you that with effect from 1st December 2016, the following categories of products will be removed from the NDA register;
i) Registered products with manufacturing sites whose Good Manufacturing Practice (GMP) has expired. ii) Registered products whose retention fees have not been paid for the Financial yeah 2016/17.
Local Technical Representatives/Licence holders who fall in the above category are advised to ensure compliance with the law comfirm the status of their products to avoid any inconvenience.
Re-instatement of the products on the register shall be done according to the established procedures, after compliance.