Signed in as:
filler@godaddy.com
Signed in as:
filler@godaddy.com
In Collaboration with IVD manufacturers our team complete the verification process of any instrument installed for clinical use.
Services provided as part of the instrument installation process.
We have a range sample types in our biobank and extensive clinical support to ensure verification of examination methods is fully compliant to ensure the validity of results pertinent to clinical decision making.
PQ will be fully completed ready for assessment from as little as 7 days saving your organization valuable time.

Premade validations sample packs delivered to conduct location evaluations of your procedure /instrument

Our team will support you as a medical laboratory in your adjustment to the IVDR and help ensure that you comply with the requirements for using LDTs whilst maintaining accreditation against the ISO 15189 standards.
Knowing the clinical context of these requirements, effective application and dissemination of knowledge is critical to ensuring minimal harm to patient on an ongoing basis.
We train on the 'why' the standards are important in clinical context, providing case studies on how non-compliance leads to detrimental healthcare.
We also focus on training clinical teams to ensure they fully understand laboratory governance requirements.
Business Service Promotion Mobile Video (mp4)
DownloadADAMTS13 diagnosis
Case studies from real cases of ? TMA conditions provided by the UK TTP registry.
For full training, contact us to provide a range of training materials on TTP diagnosis .