|
Quality Control is everyones responsibility at HC-V.
The Quality Assurance department works with each Department Manager to write Standard Operating Procedures,
which comply with federal and state method requirements.
Each analyst must complete a Documentation of Capability for the method and sign the SOP.
It is that analysts responsibility to ensure the analysis meets the method QC requirements. The department supervisor subsequently checks the
analytical batch and associated QC for method compliance. A 3rd QC check is performed by the Reporting Department for project specification compliance.
In addition, 100% of reports requiring full deliverables as well as 25% of all other reports undergo full validation-type review by the QC department.
At HC-V, Quality Assurance/Quality Control is everyones job.
The Quality Assurance department is also responsible for monitoring QC non-conformance as well as deficiencies
from internal audits
and blind samples. Any non-conformance is documented and discussed in weekly supervisor meetings. Corrective Actions are documented and implemented
immediately.
HC-V is a NELAC certified laboratory.
Certification is also maintained with the following states: New Jersey, New York, Pennsylvania,
Connecticut, Kentucky, & Massachusetts.
|
