Linkor Signature
Training and support

Implementation support for a safe, practical service.

Successful use of Linkor depends on more than the analyser itself. Healthcare providers need appropriate training, workflow support, clear patient communication and suitable governance documents.

Installation support

Support with initial setup, workflow familiarisation and preparation of the analyser for use in accordance with the manufacturer’s instructions.

Staff training

Training can cover sample collection, test preparation, analyser operation, infection control, documentation and result communication. Each provider remains responsible for ensuring that staff are appropriately trained, competent and authorised to deliver the screening service.

Clinical resources

Example documents can support consent, result reporting, patient communication and standard operating procedures — see Clinical Resources. Providers should review and adapt these materials to their own clinical governance, professional and local requirements.

Practical support

Resources available for healthcare providers.

Documents

  • Example patient information and consent wording for local review and adaptation
  • Example screening result report for integration into the provider’s own documentation process
  • Capillary blood collection workflow
  • General medical practitioner or healthcare professional communication template
  • Unboxing and setup checklist

Operational guidance

  • Stock and test-kit ordering through Regen Biologics Ltd
  • Calibration guidance
  • Basic maintenance guidance
  • Example screening pathway for local governance review and adaptation
  • Frequently asked staff questions
Video guides

Watch the setup and testing walkthroughs.

Supplementary step-by-step video guides covering reagent installation and the testing workflow. These guides do not replace formal training or the manufacturer’s instructions for use.

Reagent installation

Test procedure tutorial

Training materials, templates and workflow examples are provided to support implementation. They do not replace the manufacturer’s instructions for use, local clinical governance, professional judgement, staff competency assessment, indemnity requirements or applicable legal and regulatory obligations.

Request the healthcare provider resource pack.

Ask for example reports, consent wording and workflow documents for local review and adaptation.

Request Resources