Requirements for Accredited Laboratories
Adding or Replacing MR Systems
Required Documentation for ICAMRL Accredited Laboratories Adding or Replacing MR Systems
ICAMRL accredited laboratories are required to provide notification of either the replacement or addition of a new MR system, during their three year accreditation cycle.
The following information is required:
- A letter stating that the laboratory has replaced or added an MR system.
- Equipment information: manufacturer, model and serial number of the new unit.
- Documentation of acceptance testing performed, prior to clinical use
- Quality assurance testing
- 1 case study and final report (representative of the testing areas)
- Fee of $800.00 per unit.
Upon the ICAMRL’s review of the required information, laboratories will receive written notification regarding the continuance or suspension of their accreditation status. The laboratory’s accreditation will expire on the original date, as printed on the accreditation certificates.
Laboratories within six months of their accreditation expiration date should contact the office for guidance.
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