Category: Allgemein

Nhs Master Indemnity Agreement

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 „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. To be added to the MIA registry, please enter your business data in the fill fields under the Master Indemnity Agreement [PDF – 117Kb]. Please email this document as a PDF document to John.Slater@nhs.scot Follow the information instructions for suppliers regarding MIA membership [PDF – 688Kb] and send us the PDF agreement signed by email. Please do not print and reserve the document. The HRA will continue to use the first assessment letter and the HRA letter of authorization to clarify the proponent`s stated intent regarding the use of the MIA or the inclusion of the equipment allowance in the location agreement.

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. 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. The Master Compensation Contract (IM) is designed as a framework agreement for the requirements of NHSScotland establishments with respect to equipment and other goods delivered: if a supplier is registered with the MIA, public health services are not required to enter into individual agreements on equipment. Similarly, suppliers are not required to complete other compensation forms as soon as they have provided proof of insurance for the MIA. 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 use the MIA system in place of the equipment insurance and compensation agreement as part of the location agreement (z.B. Model Clinique Trial Agreement (mCTA), Model Agreement for Non-Commercial Research (mNCA), etc.). 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.