Once a facility or equipment has served its purpose and is no longer required, it has to be decommissioned in adherence with current legislation. The GMP Group can assist with the process of decommissioning in accordance with the Validation Life Cycle Model, which outlines the regulatory requirements for the decommissioning of validated processes, systems, equipment and facilities within the Pharmaceutical and Biotech industries.
Our team also have extensive expertise in the decontamination of all types of Manufacturing, Clinical Trial, R&D and Bulk API facilities.
Over the years we have assisted many clients in the safe decommissioning and decontamination of facilities. Consequently, the services that The GMP Group can offer within this area include Planning, Risk Assessments, Method Statements, and Tracking/Monitoring of Waste Disposal.
To speak to us further about this or to arrange a meeting, call us on 08450 344 340 or click below to send us an email.
To speak with us further about this or to arrange a meeting, please contact us:
ISO-9001
Cert no. 11289
ISO-14001
Cert no. 11289
ISO-45001
Cert no. 11289