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TCS series Distributed Temperature Control System

TCS series Distributed Temperature Control System

APLICACIONES

The automatic temperature control system of this project uses computer control technology, which can enable the process operation and parameters of pharmaceutical production to be scientifically, effectively and strictly monitored and controlled, and realize the continuity and automation of pharmaceutical production.

Características del producto

Advanced design concept

 

This project is based on the world's leading process control system SlMATIC PCS 7. This design refers to theadvanced concept of realtime release testing and implementation of product life cycle proposed by ISPE in the newversion of GlMP drug production qualitly management standard, establishes the quality monitoring system of the wholeprocess of pharmaceutical production, realizes the whole process quality management from raw materials to finishedproducts, and makes the drug production process digital, standardized, accurate, and has data Traceability functionand early warning function can comprehensively improve the quality control level of pharmaceutical production.

 

Rich experience in pharmaceutical automation construction

 

Our company has complete process research department, design and technology department, engineeringimplementation department and professional engineering installation department. We have a professional engineeringservice team. The employees have many years of pharmaceutical industry design and construction experience. Ourdesign and implementation personnel have participated in more than 100 pharmaceutical automation projects. Withsuficient design and implementation experience, we can provide users with the most professional engineering services.

 

A complete new version of GMP computer certification solutions and experience

 

Our company has a complete solution and a complete set of verification documents for computer verification in GlPAnd according to the guiding principles of international society of pharmaceutical engineering GAMP5 (productionautomation management specification), we have developed a computer system verification (CSV) template based onrisk assessment (RA). We have helped many enterprises pass the relevant verification, and we can provide fullassistance in the later GMP certification process of your company.Combined with our design experience and user requirements, the whole process automatic control of various monomereguipment in Pharmaceutical Workshop is realized, and the control system architecture network design, process flowdesign, control scheme and process control design are completed. The control program is fully in line with the single lineoperation of the product process, The modular desian is carried out of in each process. The logical relationship of eachcontrol module and the principle of real-time release are deined between each process to realize the whole productionline.

 

lmprove the stability of drug production process, realize continuous producion, meet GMP requirements in theproduction process, ensure the integrity of drug production data, improve production management level and productionefficiency, save labor costs, save energy and reduce consumption, and improve product quality.

 

 

  • Mlaintainability: the system shall be of good maintainability with a long-term and stable supply of spare parts forcomputers and templates and various sensors and actuators to be used. After our company training, the enterprise canmaintain by itself.

 

  • Scalability: the system is an open system, providing standard TCPlP data communication interface protocol,interfacesoftware and application software interface, with good flexibility and scalability, to meet the requirements of increasingproduction scale for measurement and control ability.

 

  • Security: this system has the authority mechanism, realizes the multilevel authority management, divides five diferentlevels to the operation user, different levels of user operation authority is also diferent. The control system is a relativelyclosed network, and the system network and enterprise LAN or extemal network between the configuration of a firewallcan effectively prevent viruses and network attacks, for the system to operate to create a secure environment.

 

  • Improve the stability of batches: according to the technological reguirement of batch production, establish theappro priate production model and strengthen the management of batches.Through the production batch productionplan designation, produ cion plan distribution and tracking management module, the realization of phammaceuticalproduction batch management.

 

  • Ensure that the integrity of the production data: by applying the computer management system in conformity withthe GlP standard and automatic control svstem, reaize the production of fully automatic data acquisition and monitoringeficient, accurate and complete by the computer system of colle cting and analyzing data processing, are prone to avoidthe traditional manual recording of lagging production data, missing and error.

 

  • Improve traceability of production records: traceability is GMP pharmaceutical producion data, the FDA and othernecessary content of medical industry certification, application of the phammaceutical and pharma ceutical producionauto mation control system intelig ent manufacturing qualtly infomation management system software, the batch numbergoods name, ime, equipment, operators and other pharmaceulical pro duction data in real time, complete and accuraterecords, and implement reverse retrieval process of the production data, can restore all the production status, productionenables producers to analyse the causes of defects of the quality of the products, at the same ime through data tracefunction enables pro ducers to have a better understanding of actual production status, provide data basis for improvethe production.

 

  • Energy saving and environmental protection: the application of production process and infommation managementsystem to pharmaceutical production has a signifcant effect of energy saving, at the same time reduce the intemmediatelink of pharma ceutical production, eliminate the waste of products in the production flow link.

 

◆ Sistema de control de temperatura TCU totalmente automático.
◆ Diseño e implantación de sistemas DCS.
◆ Diseño secundario del sistema de control de automatización del taller farmacéutico;
◆ Selección y suministro de equipos, válvulas e instrumentos para el sistema de control de automatización;
◆ Suministro e instalación de cables, puentes, conductos de aire y conductos de protección relacionados con el control de la automatización;
◆ Trabajos de cableado de instrumentos de sistemas de control automático, válvulas, armarios de control y cajas de islas de válvulas;
◆ Desarrollo de software de sistemas de control automático, escritura y depuración de programas de control;
◆ Responsable del ajuste de un solo instrumento, depuración de la vinculación del sistema de control automático, aceptación cualificada y entrega;
◆ Responsable de la formación técnica y el servicio posventa a los usuarios en el uso diario y el mantenimiento;
◆ Responsable de la preparación de todos los equipos, listas de materiales y presupuestos del sistema de control;
◆ Responsable de proporcionar los puntos de E/S de todo el sistema;
◆ Diseño de sala de control central de control automático;
◆ Diseño y construcción de tuberías de proceso;
◆ Suministro e instalación de sistema de agua fría;

 

APLICACIONES

New materials | Special gas production temperature control

API | intermediate production temp control solution

Distillation concentration temperature control solution

Más información

Desde nuestra fundación en 2006hemos atendido a más de 30.000 clientes y poseemos varias patentes que demuestran nuestra innovación y fiabilidad. Nuestros enfriadores son seleccionados por más de 100 universidad proyectos de laboratorio en todo el mundo y exportados a más de 20 países. Garantizamos la máxima calidad mediante un riguroso 3 pasos proceso de control de calidad: inspección visual, pruebas de rendimiento y pruebas de seguridad eléctrica. Nuestro compromiso con la excelencia está respaldado además por nuestro Atención al cliente 24/7 compromiso de asistencia. Además, contamos con agentes en Estados Unidos, Canadá, Australia, Rusia y Corea del Sur, lo que nos convierte en un socio global de confianza para sus necesidades de enfriadoras. Elija lneya por calidad y asistencia para su proyecto.
18+

Años de experiencia

30000+

Clientes satisfechos

25000

m² Área de producción

80+

Tecnologías patentadas

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