Basic Info.

Model NO.

NTD200/400/60/800/1000/1200/1500/1800/2000

Trademark

Dr. Pharm

Origin

China

Model NO.

NTD200/400/60/800/1000/1200/1500/1800/2000

Trademark

Dr. Pharm

Origin

China

Product Desciption

NTD series Lifting Feeder





Purpose:
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:




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.
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.
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.
Operational Qualification (OQ)	Documented verification that the equipment-related system or subsystem performs as specified throughout representative or anticipated operating ranges.
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.
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.
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.
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.

V SHAPE MODEL VALIDATION




Equipment Lab