IOQ for Anaerobic Cabinet
£60.00
The basis of the validation is to prove the anaerobic conditions are maintained by circulating the anaerobic gases such as CO2, H2 and N2 in addition to thermal mapping to identify risk to product that may be exposed to temperature that is unsuitable for its state and composition.
Description
The IOQ (Installation Operational and Qualification) for Incubator Validation is to ensure that the cabinet has been installed in accordance with the manufacturer’s specifications and operates correctly and is fit for use in accordance with cGLP, Health, and Safety requirements and user requirements. The basis of the validation is to prove the anaerobic conditions are maintained by circulating the anaerobic gases such as CO2, H2, and N2 in addition to thermal mapping to identify risk to a product that may be exposed to temperature that is unsuitable for its state and composition.
Our templates are developed with consultants who have over 20 years of experience in the Medical Device industry and documentation that has been through successful audits.
Our consultants are available, should you need further assistance in completing the documentation.
