The Healthcare Estates and Decontamination sector employs a number of terms and acronyms that we have used throughout this website in order to explain our services.
Below is a list of commonly used terms. For a more in-depth list of terms, please view our Terms Index page.
Authorising Engineer. These are independent engineers (appropriately qualified/experienced individuals) who are authorised to take responsibility for the management of safety guidance recommended by the Department of Health.
See our Authorising page and IHEEM page.
Authorised Person. These individuals are responsible for a specific discipline that contributes to the running of a hospital within government guidelines.
See our Roles We Help page.
Auditing Validating Monitoring. That is who we are and what we do!
See our About page for more information about AVM Services or have a browse around our website. If you don’t get the information you want, please contact us.
Continuing Professional Development. A common practice of recording the skills, knowledge and experience that professionals gain (formally or informally) as they work.
As well as providing many training courses with City & Guilds accreditation, our courses also contribute towards CPD.
Decontamination. Abbreviation often used.
See our Decontamination page.
Food and Drug Administration. A US government agency that has responsibility for decontamination (among other) sectors. The UK equivalent is The Medicines and Healthcare products Regulatory Agency (MHRA).
Health and Safety Executive. A UK government agency responsible for the regulation and enforcement of workplace health, safety and welfare.
Health Technical Memoranda. Provide comprehensive advice and guidance on the design, installation and operation of specialised building and engineering technology used in the Healthcare Estates sector.
Institute of Healthcare Engineering and Estate Management. Professional member-based engineering institute involved in implementing government policy in the Healthcare Estates sector.
See our IHEEM page.
The Medicines and Healthcare products Regulatory Agency. Regulatory authority with responsibility for the authorisation, granting, renewal, variation, suspension, and revocation of licences, certificates, or other regulatory mechanisms relating to those medicinal products and medical devices for human use which are clinically investigated, marketed, supplied, manufactured, or assembled in the UK.
National Health Service. AVM was set up by the NHS in 1989 and we have been its decontamination partner ever since.
Standard Operating Procedure. The documentation of processes that an organisation uses to ensure services (or products) are delivered consistently each time.
Sterile Services Department. Department responsible for ensuring that equipment and instruments are fit for use by the medical staff e.g. surgeons or other 'end users'.
See our Roles We Help page for further information about SSD Managers.
Documented procedure for obtaining, recording and interpreting data to show that a process will consistently produce product complying with pre-determined specifications.
Find out more about the three levels of decontamination of reusable medical devices >
If you would like to find out more about our training courses: