IPDB › China Industry › Manufacturing & Processing Machinery › Assembly Line & Production Line
New Design - Build Pharmaceutical EPC Turnkey Project with Factory Price1
Assembly Line Production Line, Pharmaceutical Production Line, Pharmaceutical Machine/Equipment, Pharmaceutical Turnkey
Shanghai Iven Pharmatech Engineering Co., Ltd.
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Product Description Customizable PP bottle Filling and Capping Production Line/ Pharmaceutical & Medical Fully Integrated PlantSHANGHAI IVEN PHAMATECH is considered as leader for IV solution turnkey projects supplier. Complete facilities to produce IV Fluids and Parenteral Solutions in Large (LVP) volumes with capacities from 1500 up to 24.0000 pcs/h. IVEN Pharmatech is the pioneer supplier of turnkey plants that provides integrated engineering solution for worldwide pharmaceutical factory such as IV solution, vaccine, oncology etc., in compliance with EU GMP, US FDA cGMP, PICS, and WHO GMP. We provide the most reasonable project design, the high quality equipment and the customized service to different pharmaceutical and medical factories from A to Z for Non-PVC soft bag IV solution, PP bottle IV solution, Glass vial IV solution, Injectable Vial & Ampoule, Syrup, Tablets & Capsules, Vacuum blood collection tube etc. Core descriptionSHANGHAI IVEN PHAMATECH is considered as leader for IV solution turnkey projects supplierIn our turnkey offers we usually exclude those items that can be procured locally at reasonable prices by the customer itself (like land, buildings, brick wall parts…).IVEN besides can provide the Turnkey project also can help client for below work:- Advanced Know How Transfer for additional Glass bottle IV solutions.- Post-Start up assistance- Raw Materials and Consumables- Black UtilitiesModelSrd1aSrd2aSrd3aSrd4aSrd6aSrd12aProduction capacity (500 ml)900 bph2000 bph2800 bph3600 bph5000 bph8000 bphPower sourceAc 380v50 hzPower(kw)82226323260Compressed air pressureDry and oil-free compressed air pressure is≥0.6 mpa,the cleanness is 5 μm.The machine will automatically warn and stop when the pressure is too lowCompressed air consumption (/min)100020002500300040007000Clean air pressureThe pressure of clean compressed air is≥0.4mpa,the cleanness is 0.22μmClean air consumption (l/min)500800900100012002000Cooling water pressure>0.5kgf/cm2(50kpa)Cooling water consumption(Vh)100300350500400800Nitrogen consumptionAccording to the customer's special requirements,can use the nitrogen to protect the machine,the pressure is≥0.6 mpa.The consumption is≤45 I/minRunning noise<75 dbRoom requirementsEnvironmenttemperature:≤26oC;humidity:45%-65%,max.humidity≤85%Overall size(m)3.26*2.0* 2.14.72*2.6* 2.15.52*2.7* 2.16.92*2.7* 2.18.97*2.7* 2.258.97*4.65 *2.25Weight(ton)3456812STANDARD IV SOLUTION PRODUCTS &TPNNaCl 0,18 - 2.7%Glucose 2,5 - 50%Sodium Lactate (Hartmanns's) SolutionRinger LactateWater For injectionSterile Water for IrrigationSodium Chloride 0.9% for irrigationSodium ChloridePotassium Chloride 0.15 - 0.3% in Sodium Chloride 0.9%Potassium Chloride 0.15 - 0.3% in Glucose 5%TPN (Total Parenteral Nutrition)Amino acidsFat EmulsionSPECIAL SOLUTIONSParacetamolPlasma ExpandersMannitolLidocainje hydrochloride 0.4% and glucose 5%Sodium bicarbonate 1.26 - 4.2%Phosphate IV solutionMetronidazoleCiprofloxacinLevofloxacinFluconazolFROM DESIGN TO VALIDATION, WE ARE ALWAYS CONSIDERATION FOR OUR CLIENT.The standards of good manufacturing practice (cGMP) require special attention to risk assessment and verification procedures: "… it is requirement of good manufacturing identify the activities of validation necessary to demonstrate control critical aspects of particular operations. The significant changes made to installations, equipment and processes, which may affect product quality, should be validated. A procedure for risk assessment should be used to determine the scope and extent of validation." The Validation Master Plan serves to make sure that all equipment, procedures, that may affect the quality or integrity or effectiveness of the product, are validated; it contains the general principles which comply during the validation task, and plans activities to be carried out for this purpose. IVEN TURNKEY FOR IV FLUIDS AND PARENTERAL SOLUTIONS / STANDARD STEPS√ Basic Engineering √ Detailed Engineering √ Design Qualification √ Inlet Water Pretreatment Plant √ Pharmaceutical Water Systems (Softened, Purified and Distilled Water) √ Pharmaceutical Processing and Solution Preparation Systems √ Pharmaceutical Bottle washing, Filling, Inspecting, Packaging lines √ Clean Rooms √ Epoxy coating of the floors/PVC floor √ HVAC and air treatment plant √ Autoclave √ Pure Steam Generator and PS circuit √ Laboratories of Analysis (Microbiological / Chemical) √ Site Master Plan √ Validation Master Plan √ Installation √ Training √ Start up √ Technical Files & Documentation √ IQ/OQ √ PQ Protocols √ Validation at Site √ Standard Operating Procedures √ Initial Know How Transfer √ GMP preAudit √ Spareparts for yearsIVEN Oversea Turnkey ProjectsTill now, we've already provided hundreds sets of pharmaceutical equipment and medical equipment to more than 40 countries. Meanwhile, we helped our customers to built the pharmaceutical and medical plant with turnkey projects in Russia, Uzbekistan, Tajikistan, Indonesia, Thailand, Saudi, Iraq, Nigeria, Uganda etc. All these projects won our customers and their government high comments.IVEN profession and experience can help you finish whole IV solution turnkey plant in the shortest time and avoid all kinds of potential risks:IVEN oversea pharmaceutical turnkey plants customers:Meanwhile, we helped our customers to built 20+ pharmaceutical and medical turnkey plants in Russia, Uzbekistan, Tajikistan, Indonesia, Thailand, Saudi, Iraq, Nigeria, Uganda, Tanzania, Ethiopia, Myanmar etc, mainly for IV solution, injectable vials and ampoules. All these projects won our customers and their government high comments.We also exported our IV solution production line to Germany.Company Profile
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