Determine Residual Oil Content Within Medical Compressed Air

BEKO TECHNOLOGIES are delighted to inform you that our METPOINT® OCV monitoring system has been successfully validated from BfArM (German Federal Institute for Drugs and Medical Devices) as a method to determine residual oil content within medical compressed air.

The validation has been executed and achieved within a strong co-operation project of a global gas company and BEKO TECHNOLOGIES.

In a joint project, the companies have validated a procedure for monitoring oil vapours in compressed air systems for medical air. The suitability of the monitoring method was validated on the basis of the requirements of the latest version of CPMP/ICH/381/95 as well as reference measurements obtained with recognised test procedures.

All measurements in this validation process were obtained using METPOINT® OCV photoionisation detectors (PID) from BEKO TECHNOLOGIES. The available data was submitted to the German Federal Institute for Drugs and Medical Devices (BfArM) as a variation subject to approval in relation to the marketing authorisation dossier.

It encompasses threshold monitoring not only of the oil vapours arising during manufacture of the active pharmaceutical ingredient (production of compressed air), but also of the filled batches of medicinal products (compressed gas cylinder). The variation was reviewed positively by the BfArM.

METPOINT OCV is therefore validated as a method to determine residual oil content within medical compressed air.

For more information on our METPOINT OCV range, please contact us on 01527 575778.

Ruth Goodison
BEKO Technologies Limited
2 & 3 West Court, Buntsford Park Road, Bromsgrove, Worcestershire, England, B60 3DX.
Tel: 01527 575778. Fax: 01527 575779.
E-mail: info@beko-technologies.co.uk
Website: www.beko-technologies.co.uk