Laboratories · Quality Control · Basic
Record readings at the same time each day. If any reading is outside spec, document corrective action and time conditions returned to range.
A weekly environmental monitoring log for US laboratories, supporting FDA GLP (21 CFR Part 58), CLIA, and CAP accreditation requirements. Record daily temperature and humidity readings in °F across analytical labs, instrument rooms, balance rooms, and storage areas.
Documented environmental monitoring is a regulatory requirement and a common finding in FDA and CAP inspections. This log provides the evidence that lab conditions were maintained within validated ranges.
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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