Validation of Blood Storage Equipment now available from Vindon Scientific

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Click here to download the new guidelines

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Those who work in regulated industries such as pharmaceuticals and medical devices have extra responsibilities that are generally not found elsewhere, it involves compliance to guidelines set by both the industry and regulatory bodies such as the FDA. The guidance covers GMP, GAMP, Euro directive 6, Change Management, 21 CFR Part 11, Software Verification, Process Validation, Equipment Validation.

Vindon Scientific's service and validation solutions ensure your equipment gets the attention it deserves. We have engineers throughout the UK on hand to respond to call outs received via our service centre

Maintenance

Equipment needs regular maintenance to remain in optimal working condition. Maintenance regimes can be tailored to individual requirements to suit different products and budgets. The most comprehensive is the Vindon Scientific Premier Service which is tailored to suit the user's specific requirements with regard to inclusive service visits and calibration details.

If a problem occurs, one phone call to our Service Office number will ensure either telephone advice on how to resolve minor problems or site attendance of one of our trained Service Engineers within 24 hours to rectify the fault.

Contract maintenance packages offer complete peace of mind. Our Premier and Standard contract holders receive priority attention at all times.

Alternatively you may only require a contract covering the annual calibration and an inspection visit.

Calibration

Regular calibration of control, indication and recording systems is essential to ensure the accurate and repeatable performance of an environmental cabinet.

Vindon Service Engineers are trained in single point calibration. All test meters are regularly calibrated to UKAS standard and calibration certificates provide an audit trail back to national standards.

The calibration service can be a one off visit or part of a service package. The frequency of calibration is usually once a year but some critical applications are calibrated bi-annually.  Vindon offer a flexible approach, tailored to each individual customers needs.

Validation

We offer a full on-site Validation Service for Environmental Rooms and Chambers and all associated equipment (data logging systems, chart recorders, etc.).

All reference standards are regularly calibrated by UKAS accredited laboratories and are traceable to national standards.

Performance mapping tests can be executed for temperature, humidity and light distribution. All documentation is designed to show compliance with ICH guidelines and to meet FDA requirements.

If you would like to see the Data Loggers and Chart Recorders we have available - you can see them here.

Vindon Scientific Limited - Tel:.+44(0)1457.876616..Fax:.+44(0)1457.871355 Registered in England No. 878160

Vindon Scientific Ltd can provide it’s customers with a wide variety of external services.