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Detailed Project Report On Manufacturing Of Sterile Water For Injection | |
| SWFI (Sterile Water for Injection, USP) is sterile water for injection that has been purified by reverse osmosis and deionized using modern technologies to meet or exceed USP criteria for sterility, physical characteristics, and purity. The ionic content of SWFI is less than 10 mg/L. (TDS). Water is frequently utilised in therapeutic applications as a vehicle or dilution for other drugs. SWFI (Sterile Water for Injection) is sterile water that has been sterilised and disinfected to be used as an injection. SWFI is used to deliver injections to patients or to prepare and clean an area before providing an injection in both hospitals and doctors' offices. Sterile Water for Injectable (USP) is a sterile, non-pyrogenic injection water. The pH ranges from 3.5 to 7.0, with an osmolality range of 50 to 300 mOsm/kg (calc). The most common sterile preparations are solutions or suspensions, however solid pellets for tissue application are also possible. Parenteral drug manufacture has evolved into a highly specialised field of pharmaceutical processing. The backbone of sterile formulation and/or pharmaceutical dosage form is sterile facilities for all pharmaceutical products, particularly parentral preparation. It is critical to maintain sterility in all locations where the formulation process is carried out, from the beginning to the end. Because they are injected directly into the bloodstream, sterile injectable products are extremely important and delicate. Sterile Water for Injection is only intended to be used as a solvent or diluent vehicle for parenterally delivered medications or solutions, as well as a source of water for parenteral fluid replenishment once appropriate additives have been added to prevent blood tonicity. It can be used as a lavage or rinsing agent in some circumstances, although if available, isotonic solutions adequate for the area of exposure are preferred. Sterile Water for Injection provides a supply of water for parenteral fluid replenishment when adequate osmolarity has been attained when supplied intravenously as a medication vehicle. By 2025, India's biotechnology industry, which includes biopharmaceuticals, bioservices, bioagriculture, bioindustry, and bioinformatics, is predicted to develop at a 30 percent annual pace to reach US$ 100 billion. The rise in lifestyle disorders such as diabetes and heart disease has increased demand for pharmaceuticals in India. India has a big reservoir of scientific and research talent, as well as a large population with high cancer and chronic disease rates. India is a suitable location for drug research and clinical trials due to its shorter recruitment timeframes and reduced expenses. By 2025, the Indian pharmaceutical sector is estimated to be worth US$ 100 billion, while the medical device market would be worth US$ 25 billion. In FY20, India's pharmaceutical exports totaled US$ 20.70 billion. Bulk pharmaceuticals, intermediates, drug formulations, biologicals, Ayush and herbal items, and surgical products are all examples of pharmaceutical exports. Key Players • Albert David Ltd. • Amanta Healthcare Ltd. • Chandra Bhagat Pharma Ltd. • Denis Chem Lab Ltd. • Health Biotech Ltd. • Ivy Health & Life Sciences Pvt. Ltd. | |
| Plant capacity: Ampoules 5 ml Size: 200,000 Nos. per day | Ampoules 10 ml Size: 150,000 Nos. per day | Ampoules 20 ml Size: 150,000 Nos. per day | Plant & machinery: 19.33 Cr |
| Working capital: - | T.C.I: Cost of Project: 30.40 Cr |
| Return: 27.00% | Break even: 39.00% |
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