Specification
Vindon has been manufacturing controlled environment chambers for over 40 years and it is these units, with proven reliability and very accurate control of temperature and humidity, that are used in the Vindonwestech storage suite.
- Purpose built stability storage facility close to all transit links (airports & road networks)
- Vindonwestech service professionals on call at all times
- Spare running and validated disaster recovery cabinet
- Backup generator
- 24/7/365 facility support & maintenance
- In house Eurotherm data logging & monitoring system (NIST Traceable)
- Full system redundancy with backup system in house
- Data backed up offsite daily
- FDA Title 21 CFR part 11 compliant monitoring system.
- System validated
- Over 60 years combined experience within the group
- Dedicated QA/QC department within the group
- ISO 9001 compliant (est. certification Dec 2010)
- Cabinets validated to ICH standards
- Detailed reports available
- Scheduling system for client pull returns
- Full confidentiality of samples at all times. i.e. All projects are labeled with a project and client assigned name
- Same day or next day sample returns to anywhere in the contiguous USA
- All shipments are assigned an individual tracking number
- A full complement of temperature controlled shipping packages including -20C and Dry Ice
- Data logged transport of samples to monitor compliance
- Partnership with global logistics leader
- Full alarm system including motion and smoke detectors will monitor the facility environment every second of every day
- All access points in the building will have alarm contacts
- Closed circuit television monitors the outside of the building for personnel or vehicle activity. Providing a safe and secure environment for all samples
- Cabinets physically locked at all times
- Cabinets located with an access controlled part of the facility, restricted down to trained authorized staff
All of our Ultra-low chambers are services and validated annually
Vindowestech's Ultra low temperature secure storage chambers are ideal for biological and pharmaceutical products.
The chambers are validated annually with all the documentation being pre-authorised for use prior to the commencement of the validation. The validation and associated documentation are completed by trained Vindonwestech engineers. The completed documentation is checked by another validation engineer before a final check and approval by the Vindon QA department.
Our in-house service engineers service the chambers annually, inline with Vindonwestech's rigorous service procedures.
All of our chambers are continually monitored via our CFR 21 part 11 compliant data acquisition system. The validated data acquisition system will alert our on-call team if any deviations outside the specification limits.
E.g. -80ºC (-5/+7ºC) Any reading above -73ºC or below -85ºC will alert our on-call team to respond to site within two hours - and in the event of a chamber failure, Vindonwestech has spare dedicated and validated chambers to allow for the controlled movement of your product, protecting its integrity at all times.
Click the images below to view our Low temperature & Ultra-low temperature chamber validation traces
