Clinical testing laboratories that perform testing in the United States must comply with Clinical Laboratory Improvement Act (CLIA) requirements.
Compliance with CLIA regulations already requires a sizeable financial investment by clinical laboratories, so every additional dollar spent on compliance costs can affect the bottom line and add to the already-high level of complexity. Yet it isn’t uncommon for compliance expenditures to be unnecessarily excessive.
This white paper, “Managing CLIA Compliance Costs: 6 Mistakes Every Laboratory Should Avoid,” lays out how to avoid the 6 most common – and costly – mistakes that clinical testing labs make when seeking compliance with CLIA regulations:
- Spending Too Much on Documentation Management
- Spending Too Much on Training
- Spending Too Much on Customer Complaints Management
- Spending Too Much on Audit Expenditures
- Spending Too Much on Change Control
- Spending Too Much on CAPA Management
Offered Free by: MasterControl Inc.
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