KAMAL BHATT

I have over Seven and a half years of experience in the formulation Documentation of pharmaceutical products. I have worked in a variety of Pharmaceutical Products , production, and quality control. My experience includes developing of formulations, pharmaceuticals products. In my previous roles, I have significantly enhanced product quality and consistency.

• Two years and six months, Formulation Documentation Department, Copmed Pharmaceutical Pvt. Ltd., Dehradun
• One year, F&D Department, Rusan Pharma, Dehradun
• One year, F&D Department, Windlase Biotech, Dehradun
• Two years, F&D, Akums Drugs & Pharmaceutical Ltd., Haridwar
• One year and three months, Pharmaceutical Production Department, Intas Pharmaceutical Limited, Dehradun
• Eight months, M.Pharma project work in F&D, Sharon Pharma, Dehradun
• One month, Industrial training in production, Mepramax Pharma, Dehradun

• Compression machine
• Coating machine
• FBP
• Blender
• Co-mill
• Bilayer compression
• Tablet in tablet compression machine
• All equipment that are used in the formulation and preformulation study of tablet

Formulation & Evaluation of tablet in  tablet of Famotidine with antacid.

• MHRA
• Health Canada
• TGA
• South Africa audit

Hindu

• Date of Birth: 01/01/92
• Gender: Male
• Nationality: Indian
• Marital Status: Unmarried

• English
• Hindi

• Research Article on Formulation and evaluation of Bilayer tablet of Famotidine with antacid layer, Indo American Journal of Pharmaceutical Science
• Review Article on Oral sustained release drug delivery system: a concise review, World Journal of Pharmaceutical Research

Playing & watching cricket

I hereby declare that the information furnished above is true to the best of my knowledge.

F&D Documentation

• Maintain all the Documents and equipment related to FRD.
• Talk to the vendors regarding procurement of material.
• Coordinates with the analytical department for formulation related issues.
• Literature search and preformulation study of given formulation.
• Take trial of OSD, record and maintain related documents like Lab notebook or log books.
• Prepare Stability Protocol, FPS, MFR, PDR, PRR of formulation of OSD.
• Involve in scale up of formulation.
• Handling of validation batches.
• Do technical transfer of OSD.
• Maintaining of all documents related to manufacturing areas as per cGMP, MHRA, TGA.
• Preparation of Daily Production report and manpower allocation.
• Active calculation and Batch Reconciliation on various stages.
• In process checking on various intermediate stages.
• Review of Batch Manufacturing record and other related documents for its completion of various intermediate and final stages.