Laboratories · Quality Control · Intermediate
Maintain one log per instrument. Record every calibration event including routine checks and full recalibrations. Attach calibration certificates where applicable.
A calibration tracking log for US laboratory instruments, supporting FDA GLP (21 CFR Part 58), CLIA, and CAP accreditation requirements. Record calibration dates, NIST-traceable standards used, results, pass/fail determination, and next due dates for each instrument.
Proper calibration documentation is critical for regulatory inspections, proficiency testing, and ensuring the validity of analytical results. This log provides the audit-ready format FDA inspectors and CAP assessors expect.
This checklist template is provided as a general-purpose resource and is not tailored to the regulatory requirements of any specific country, region, or jurisdiction. It is the responsibility of each organisation to review and adapt this template to ensure compliance with all applicable local laws and regulations. Miratag does not accept liability for any inaccuracies or omissions, or for any actions taken based on this template.
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