The „MIA conditions“ have been updated to respond to changes in departmental legislation and policy. The „MIA Appeal Agreements“ and „MIA Intermedary Agreement“ have been updated to support changes to the mia terms update. „MIA Data Protection Protocol“ is a new document that has been introduced to help health authorities comply with the general data protection regulation. The Master Compensation Register is a list of suppliers that have entered into an agreement with NHSScotland to compensate NHSScotland for liability if they receive devices from a supplier on credit, free or trial (without financial payment). If suppliers are registered in the MIA and have liability and liability insurance for valid products, as stated in the register, a MIA delivery voucher must be signed to confirm the acceptance of the goods in accordance with the terms and conditions of the MIA. The MIA delivery bulletin is the only documentation to be signed when suppliers receive devices or goods in the register. MIA is an agreement between NHS organisations in England and suppliers that provide devices free of charge, either on loan or in the long term. If a supplier is registered in the MIA, public health services are not required to enter into individual agreements for the devices. Similarly, suppliers are not required to complete other compensation forms as soon as they have provided proof of insurance for the MIA. MIA is an agreement between NHS organisations in England and suppliers that provide devices free of charge, either on loan or in the future. Registering a supplier with the MIA gives NHS organizations the guarantee that the supplier has public liability insurance to cover its debts related to the supply of its equipment. NHS organizations can enter into appeal agreements with suppliers registered with the MIA, thus offering both parties the protection offered by the plan.

In order to accept equipment or goods provided by suppliers that are not registered, boards of directors are required to enter into individual and separate agreements for goods delivered on a loan, free or trial basis. The House is not obligated to sign other documents that may be submitted by a supplier. In this case, the standard form of compensation [PDF – 70Kb] must be signed. Therefore, suppliers who regularly work with NHSScotland should consider registering to avoid having to sign separate forms when providing „free“ devices. The standard form of compensation should not be used when compliance with RGPD legislation is required. The latest update confirms that the MIA is not appropriate when the equipment is undergoing a clinical review (where insurance and compensation agreements should be concluded under the Clinical Investigation Agreement (MCIA) model. It further states that the MIA may be suitable for use when equipment is made available to a research project, if the equipment is not researched. This allows the sponsor to replace the MIA system in place of the equipment insurance and compensation agreement as part of the location agreement (z.B.