Our service

Centre Testing International Co., Ltd. (CTI) is the pioneer and leader in the TIC Industry which provides one-stop solutions on testing, inspection, certification, calibration, audit, training & technical services.

 

By Industry

Our service capabilties cover the upstream and downstream of the supply chain including textile and apparel,toys,electronic appliances,medical health,food...andother industries.

Specialty

Comprehensively guarantee quality and safety, promote compliance and innovation, demonstrate brand competitiveness, and achieve higher quality, healthier, safer, and greener sustainable development.

AUTHORITY & TRUST
QUALITY & VALUE
Pharmaceutical Instrumentation and Software System Validation

CTI provides you with pharmaceutical instrumentation and computerized system validation services, which can perform GMP validation on warehouses, box equipment, instruments and computerized systems in accordance with the GMP regulations and guidelines of various countries, combined with the needs of users, and has a professional GMP validation team, high-standard testing equipment, and a perfect quality management system.

Pharmaceutical Instrumentation and Software System Validation

Equipment Validation

CTI, in accordance with the GMP regulations and guidelines of various countries, JJF, GB and other requirements, combined with the user's actual use of the scope, to provide storage temperature and humidity, refrigerator/incubator/sterilization cabinets and other chamber parameters (temperature, carbon dioxide, pressure, etc.) performance confirmation services to ensure that the warehouse, the chamber in the normal operating methods and process conditions can be sustained.Under normal operating methods and process conditions, we can continuously meet the established acceptance standards.
 

Refrigerator

 

Incubator

 

Stability Chamber

 

Sterilizer

 

Cold Storage

 

Normal Temperature Storage

 

Analytical Instruments and Computerized Systems Validation

CTI provides full validation cycle services (including URS, VP, RA, FS, CS, DQ, IQ, OQ, PQ, VSR, etc.) from validation plan to final system release according to the requirements of GMP regulations and guidelines such as GAMP5 Risk Benchmarking, and in combination with the user's actual needs, in order to prove that the computerized system meets the user's needs and works stably in the long term, and meets the requirements of data integrity. data integrity requirements

Type

Analytical instruments and workstations

Large laboratory management systems

CSV Service

 Analyst Software for Sciex LCMSMS

 Empower 3 CDS

Easy2Sync Backup Software

SDS Software for Thermo PCR

Vaisala Veriteq CMS- Viewlinc

Gen5 Data Analyst Software

For more information please contact staff...

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