1) Assisted in the preparation of regulatory submissions and responses to health authority inquiries.2) Gained hands-on experience in dossier preparation, compilation and formatting for ROW market andsome countries of the European market. 3) Liaised with regulatory agencies, addressing queries, and facilitating communication to ensure smoothregulatory processes.4) Demonstrated strong knowledge of ICH guidelines and compliance with regulatory requirements.

1) Gained valuable experience of working of a pharmaceutical company by assisting in Formulation andQuality control department.2) Hands on experience of operating HPLC, GC-MS, LC-MS, ICP-MS, Fluidized bed dryer, Ganson coater, Rotary tablet press, High shear mixer granulator, Dissolution testing apparatus etc.3) Carried out lab scale development of solid oral dosage forms and oral suspensions