-Formulation Development of Dosage forms.-Responce to the Regulatory Query.-Documentation related to the product development-Technology Transfer of the products

•Formulation Development of Products for WHO, IRF markets•Literature survey, Preformulation studies and process development for dosage forms.•Preparing Tentative formula by literature search and taking trials for the execute experiments of lab batches under direction of Research scientist according to cGMP guidelines.•Approval of the developed dosage form as per Marketing Team requirement.•Keeping track of stability schedule for the developed formulations.•Monitoring scale up batches during technology transfer to the production sites.•Improvement in existing formulations and possibility of new dosage forms, cost reduction /margin improvement etc.•Preparation of Master Formula Records (MFR), Stability protocol, Development reports, Specifications, DCGI CTD, Product Query Response, Import License Docs etc.•Contact with different external organization as per the product development requirement for technical support.•Providing the details for material for costing & procurement. •Executing up-gradation of process technology for product quality improvement to fulfill with the requirements.