To conduct panel inspections with team of experts and member of licensing and registration board to check the implementation of WHO guide line of good manufacturing practices, good laboratory practices and good storage practices, to take sample of suspected drugs for test analysis and raid on un-registered and spurious drugs and lodging FIR to arrest them with help of police or FIA police and preparing cases for licensing and registration board after complete investigation for seeking permission to prosecute in drug court ,to regulate price control during market survey,to conduct panel inspection with the experts for grant of new DML,renewal of DML etc many more activities like attending drug court ,high court and coordination with provincial govt. members of community medicines.

to manufacture syrup,tablet and ointment as per GMP requirement of their registered product and was taking work from worker with strict GMP compliance and was preparing program for arranging raw material ,packing materials.material management,workers management and time management etc