Mubashar Iqbal Email and Phone Number

• Preparation of Registration Applications of New Molecules and CTD for WerrickPharmaceuticals• Preparation of Consumption cases for Controlled Substance• Pricing• Preparation of Quota Allocation files for controlled Substances• Preparation of Renewal files of Registered Products• Preparation of Requirement of Active Pharmaceutical Ingredients (From-6)• Updating online record of 2D Matrix on DRIS • Maintaining & Updating Record of Distributor Licenses (Specially NarcoticsSelling Licenses)• DRAP Correspondence• Post Registration Variations

In process checking, Inspection according to the guidelines of GMP in Ampoule,oral, sterile powder section(Lyophilized Section) and parenteral section.• Physical Testing.• Dispensing - Line Clearance/inspection of dispensing -Batch manufacturing,• In process Checking during optical checking & packing.• Documentation with cleaning reports, area inspections at every step ofmanufacturing. - Conducting Deviations CAPA, validation.

• Dispensing of prescription and over-the-counter medicines to the public.reviewing prescriptions from doctors to ensure accuracy and suitability forthe patient, including the dosage, ingredients required, and correctly andsafely labelled.• Managing Pharmacy staff and Training of technicians.• Ordering pharmacy supplies and controlling the inventory on a daily basis.• Maintaining an approved drug and controlled substances list and verifyingexpiry dates.• Monitoring product displays and shelves, as well as the general appearance ofthe pharmacy.• Addressing customers' requests and complaints

. Dose calculation. Inventory Control Management. Dispensing of Medicine at Pharmacy. Patient Medication History in wards

ResponsiblitiesQulaity Controlsample testing USING SPECTROPHOTOMETERDocumentationMAking DilutionsDisintegration appratusRAW MATERIAL STORereceiving and analyzing materialtaking samples from quarantineD Raw materialhandle rejected materialmoving relaeased material to storage sectionDispensing of Raw materialsProductionLine clearancearea cleaningsample preparationSupervision of workerstaking and verifying the sampleDOCUMeNTATIONbatch manufacturing recordin process control testsweight variationfriability testdisintegration testhardness testMicrobiology LAbClass A, B, C, D Area, Sterile AREA, HEPA FILTERS, distilllation processdifferent micoorganisms and culture mediaQuality Assurancelearned to control (initiation, reviewing, updating, issuing, superseding) of all documentation, i.e. SOP's, technical agreements, master manufacturing & packaging, raw material and packaging material specifications, site master file, quality manual, quality management reviews and quality risk assessments