Pharmaceutical & Biological:-Registration application submissions on CTD for Pharmaceutical, Biological and Imported products-Dealing with multiple Toll partners for Product registration-Export Registration submission to DRAP-Pre-Approval and Post-Registration Variation submissions-Renewal Submissions of Drug products (both Local and Imported)-Query responses to DRAP-Maintaining compliance with local and international regulations-Extensive review of DRAP DRB Meeting minutes for process improvement-Archiving of data in both soft and hard copy-Product document review as per relevant registration guidelinesMedical Devices and Health & OTC:-Enlistment of Medical Devices-Enlistment of Health and OTC products (Local, Imported and Toll manufacturing)-Company Enlistment of Health and OTC products (both Local and Imported)

-Dossier preparation as per CTD format for Pharmaceutical and Biological products-Dossier preparation for various Toll manufacturing partners-Query response submission to DRAP-Export registration submissions to DRAP-Maintenance and record keeping of all relevant important data-Artwork review as per International and local guidelines

- Study of manufacturing of different dosage forms