Governance and Compliance
PURA DIAGNOSTICS is undertaking accreditation with UKAS ISO EN 17025 and registration and compliance with the Care Quality Commission.
Quality Management Group is responsible for coordinating the quality management system for PURA DIAGNOSTICS Laboratory Services. The Quality Management Group’s responsibilities include:
•The organisation and direction of PURA DIAGNOSTICS Quality Management System (QMS), in line with the appropriate regulatory bodies (e.g. CQC and UKAS ISO EN 17025)
•Review internal quality assurance and external quality assessment
•To ensure sufficient resources are committed to the QMS
•To review audits including turnaround times, training and adverse events
PURA DIAGNOSTICS participates in relevant accredited external quality assessments schemes. These schemes and the corresponding disciplines are:
- Routine and Esotric Biochemistry (Blood & Urine)
In addition, our data protection, information security and business security standards demonstrate our commitment to best practice ensuring we maintain rigorous levels of compliance in every area of our work.
Training and Development
DIAGNOSTICS is committed
to the training and development of its staff, all of which undertake a
comprehensive induction and training program.
This is complemented by annual competency assessments and mandatory training packages. Assessments of Competence are undertaken to ensure all new members of staff are quickly integrated into the laboratory not only perform safely and competently.
All practicing scientists are registered with the HCPC and are educated to MSc level. All HCPC registered scientists must undertake continuing professional development (CPD) to maintain fitness to practice and as such PURA Diagnostics utilises the Institute of Biomedical Science’s (IBMS) CPD scheme to monitor and achieve this.