I would be glad to write this report for you. i am an MBa with an electronics engineering background and understand both the technical as well as business related aspects of pharmaceutical manufacturing.
Whether the process relates to the production and synthesis of drugs and processes like milling, drying, compression and coating required at different steps, or whether it is a newly discovered drug and its manufacturing is being implemented, or whether it has been passed by FDA, I will include all these isues. Moreover, I shall write about GMP (Good manufacturing practices) which regulate record keeping, personnel qualifications, sanitation, cleanliness, equipment verification, process validation or complaint handling. for new drugs, systhesis, formulation, process development and scale-up, and finally manufacturing.
I shall try to cover all sorts of pharmaceutical products like injectables, capsules, Inhalents, syrups, Lozenges, Chewable tablets, Effervescent tablets, Multi-layer tablets, Capsules, Hard gelatin, Soft gelatin, Powders, Inhaled, Aerosol, Metered dose inhalers, Dry powder inhalersFrom arrival of raw material to packaging, I shall describe the whole process. I shall dwell on maters like Form Wet granulation, milling, blending Fluid, Bed Dryer lubrication, tableting, coating, imprinting, Process combines the drug and excipients into the dosage form Excipients, API crystallization filtration, oven drying, Dry granulation, Direct compression to Quality factors.