Basic Info.
Model NO.
NTD200/400/600/800/1000/1200/1500/1800/2000
Type
Pharmaceutical Milling Machinery
Finished Dosage Form
Granules
Product Description
NTD series Lifting FeederPurpose:The machine is mainly used for conveying solid materials in the pharmaceutical industry. It can work with the wet type granulator, capsule filler, tablet press, packaging machine, etc. It is also widely used in such industries as medicine, chemical industry, food, etc.Working Principle:The machine is mainly composed of column, operation box and lifting system. When it works, push the silo into the crotch. Start the lifting system to lift the silo to a certain height, rotate the column horizontally to the process position, start the lower button to automatically lower the silo to the required position, open the butterfly valve, and realize the next procedure.Structural Feature:The machine adopts the most advanced design concept of SAR LABORTECNIC Company, and the column is made of special channel steel.*The machine adopts integrated control technology to realize stable and reliable performance.*The lifting and driving system can adopt such driving modes as hydraulic lifting, mechanical lifting, etc.*It optimizes production processes, lowers labor intensity and reduces dust pollution.*It meets FDA/cGMP requirements.Technical Parameters:
NTY series Moveable Lifting FeederPurpose:The machine is mainly used for conveying solid materials in the pharmaceutical industry. It can work with the wet type granulator, capsule filler, tablet press, packaging machine, etc. It is also widely used in such industries as medicine, chemical industry, food, etc.Working Principle:The machine is mainly composed of moveable cart, column, operation box and lifting system. When it works, move the lifting machine to the position where the equipment to be connected is located, and lock the lifting machine conical copper and transfer copper with rapid clamps. Start the lifting system to lift the transfer hopper to a certain height and turn it for 180°. Manually push the equipment to the process position of the equipment to be connected. Start the lower button to automatically lower it to the required position, open the butterfly valve, and realize the next procedure.Structural Feature:*The machine adopts the most advanced design concept of SAR LABORTECNIC Company, featured by small floor space, simple operation and good practicability.*After the transfer hopper is lifted to a certain height, it can be rotated at any angle for the convenience of feeding and connection, featured by good safety and reliability.*It optimizes production processes, lowers labor intensity and reduces dust pollution.*It meets cGMP requirements.Technical Parameters:
NTC series Lifter Among FloorsPurpose:The machine is mainly used for conveying solid materials in the pharmaceutical industry. It can work with the wet type granulator, capsule filler, tablet press, packaging machine, etc. It is also widely used in such industries as medicine, chemical industry, food, etc.Working Principle:The machine is mainly composed of machine column, fixed chassis, safety fence and upper and lower floors double-control lifting system. When it works, it pushes the materials or transfer hoppers to the lifting platform. Close the safety fence, and start the ground floor lifting program. After it reaches the designated position, start the upper floor control program, open the fence and transfer the materials or transfer hoppers to the required work station.Structural Feature:*The machine adopts the most advanced design concept of SAR LABORTECNIC Company, optimizes production processes, lowers labor intensity and reduces dust pollution.*With high safety performance, it is provided with upper and lower floors limit protection device and safety positioning lock.*The machine is provided with the acoustic and optical alarm indication function in case of rise or fall to the designated position.*The machine is provided with overload self-protection function and alarm indication function.*It meets cGMP requirements.Technical Parameters:VALIDATION DOCUMENTATION| Terminology | Defined Meaning |
Validation Plan (VP)
| This document supports the VMP, but provides the detailed validation requirements for a specific piece of equipment. |
User Requirement Specification (URS)
| This document describes what the equipment is intended to do and all essential requirements such as production rates, operating ranges, etc. The owner usually develops this document. This document links to the PQ document which tests for each of the requirements.
|
Functional Requirement Specifications (FRS)
| This document describes the detailed functionality of the equipment. The supplier usually develops this document. This document is linked to the OQ document which tests for each function.
|
Design Specifications
(DS) | These documents describe the equipment in sufficient detail to enable it to be built. These documents are linked to the IQ document that tests for all design requirements.
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Design Qualification (DQ) or Design Reviews
| Planned and systematic review of specifications, design, and development throughout the life cycle. Design reviews evaluate deliverables against standards and requirements, identity problems, and propose required corrective actions.
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Installation Qualification (IQ)
| Documented verification that all key aspects of the hardware and software installation adhere to appropriate codes and approved design intentions and that the recommendations of the manufacturer have been suitably considered.
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Operational Qualification (OQ)
| Documented verification that the equipment-related system or subsystem performs as specified throughout representative or anticipated operating ranges.
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| Factory acceptance test (FAT) | Documented verification that the equipment-related system or subsystem performs as specified throughout representative or anticipated operating ranges at manufacturer factory before shipment to end user's workshop.
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Site acceptance test
(SAT) | Documented verification that the equipment-related system or subsystem performs as specified throughout representative or anticipated operating ranges at site in end user's workshop.
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Performance Qualification (PQ)
| Documented verification that the process and / or the total process-related system performs as intended throughout all anticipated operating ranges while operating in itsspecified operating environment.
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Commissioning
| A well planned, documented, and managed engineering approach to the start-up and turnover of facilities, systems, and equipment to the End User that results in a safe and functional environment that meets established design requirements and expectations.
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Address:
Yangfang Industrial Area, Changping District, Beijing, China
Business Type:
Manufacturer/Factory
Business Range:
Health & Medicine, Manufacturing & Processing Machinery
Management System Certification:
ISO 9000, GMP
Company Introduction:
Established in 1999, Beijing Hanlin Hangyu Technology Development Inc., also known as Dr. Pharm, is a high-tech enterprise, we now has more than 500 employees, and pride ourselves as a professional pharmaceutical machinery manufacturer for solid dose. Our company has built factory buildings of more than 50, 000 square meter, and successively introduced nearly hundred sets of CNC machine equipment, which provides guarantee for delivery cycle and product quality and lay a sound foundation for future development.
As for products, our company has improved the granulating line, procedure transfer equipment, mixing equipment, coating and cleaning equipment. We purchased Spain SAR Labortecnic company and introduced its products and technology. Our company has also established laboratories meeting GMP requirements to provide users with convenience for process tests. By over a decade of fast development, we earned a nice reputation and fame in domestic market, and aims to build up the famous brand as "Dr. Pharm Precision Machinery" in fellow companies home and abroad.
Adhering to the concept of "sincerity, efficiency, innovation and prominence", Dr. Pharm is developed to the pharmaceutical industry and provides solid dose drug manufacturing factories with complete-set equipment solutions while making our contributions to the human health cause.
