Equipment Validation - Vindon Scientific Ireland

Vindon offer a comprehensive range of on-site Validation Services using reference standards that are routinely 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 provide compliant evidence of ICH guidelines and to meet FDA requirements.

Equipment Validation ensures that equipment is appropriate for its intended use.

Typical validation phases are:

Installation Qualification (IQ)
Undertaking and documenting the installation of the selected piece of equipment.

Operational Qualification. (OQ)
Performing testing of the selected piece of equipment to ensure that it meets the functional and performance specifications.

Performance Qualifications (PQ)
Multipoint performance testing of the system to ensure it always performs as intended for the selected application.

Vindon Scientific Limited performs temperature and/or humidity mapping studies utilising the latest technology. These studies are conducted to demonstrate that temperature and/or humidity controlled equipment is maintaining the specified temperature and humidity ranges.

Vindon Scientific Limited validates:

• Environmental Rooms and Chambers
• Data logging equipment
• Chart recorders
• Incubators
• Refrigerators
• Freezer
• Blood Banks
• Plasma Freezers