Designed and built to comply with and exceed FDA and GMP standards and to satisfy the demands of the pharmaceutical industry regulation, Tablex-PRO metal detection systems provide mobile, fully integrated product inspection and rejection systems for tablets and capsules.
Tablex-PRO pharmaceutical inspection systems utilise high frequency operation to provide the highest attainable metal detection sensitivity to all metal contaminants. Difficult to detect non-magnetic stainless steels and irregular shaped contaminants such as minute pieces of sieve wire and swarf are readily detected and rejected with ease.
Exceptional performance in pharmaceutical process environments is enhanced through robust construction techniques enabling previously unseen levels of on-line stability to be attained.
The compliance needs of 21 CFR part 11 are fully met through the provision of dual-level, high security log-in facilities for operators and the capture of electronic signatures and other process data.
A choice of advanced failsafe reject devices including side diverter and lift flap options are available ensuring any contaminated product is rapidly removed from the product flow.
Tablex-PRO detectors utilise Profile software technology which incorporates continuous Condition Monitoring functionality to assess key component performance and to give advanced warning of adverse trends which could lead to equipment failure if left unaddressed. Early warnings can be communicated via SMS text messages or email to key operational personnel.
Features and Benefits
|Unrivalled sensitivity and stability
|The maximum capacity to detect all metal contaminants combined with robust, on-line stability to minimise instances of false reject events
|Full 21 CFR part 11 compliance
|High security, dual level operator log-in facility with full electronic signature capture ensures full regulatory compliance to be met
|Failsafe reject systems
|A choice of genuine failsafe reject systems is available including side diverter and lift flap options
|Hygienic, easy clean design
|No tools required for dismantling/assembly. Fully submersible contact parts for easy cleaning
|Performance validation software
|Built-in performance validation software indicates when scheduled testing is due and assists QA staff by guiding them through step by step test routines
|Easy to use
|The intuitive Profile full colour touch screen operator panel provides easy set up requiring minimal operator training and reduced downtime between product changes
|Pharmaceutical construction standards
|Designed and built in mirror finish stainless steel to comply with 21 CFR parts 210 & 211
|Built-in condition monitoring
|Constant analysis of the detection coil and electronics systems provide advanced warning of potential problems prior to failure enabling planned maintenance routines to take place
|SMS and email communications facilities
|Communication of key production process messages for maintenance and QA procedures maximises uptime and manufacturing efficiency
|Can be provided with an integral Ethernet adapter enabling connection to all external data collection devices and factory management systems