NASPO Certified
NASPO Certified
Field Eagle gives pharmaceutical and life sciences operations teams the tools to manage GMP compliance inspections, equipment qualification records, facility condition assessments, and quality audit programs across manufacturing facilities, laboratories, and cleanrooms. Digital inspection workflows replace paper-based processes, 21 CFR Part 11 compliant electronic records are maintained automatically, and FDA audit-ready documentation is retrievable instantly. AI Preventative Maintenance identifies critical manufacturing equipment approaching failure before it causes batch losses or production shutdowns.
Tablet-based and fully offline. FDA, GMP, ICH, and 21 CFR Part 11 compliance documentation. NASPO ValuePoint approved.
Pharmaceutical manufacturing operations require the most rigorous and documented inspection programs of any industry due to the direct impact of equipment and facility condition on product quality and patient safety.
Cleanroom condition assessments, HVAC qualification monitoring, environmental monitoring program documentation, and facility cleanliness inspections. All documentation maintained per FDA 21 CFR Parts 210 and 211 GMP requirements.
Equipment qualification inspection records for IQ, OQ, and PQ documentation. Preventive maintenance inspection programs for manufacturing equipment linked to specific asset records. Calibration due date tracking and calibration record management.
Laboratory equipment maintenance inspections, biosafety cabinet certification records, fume hood inspection programs, and laboratory safety compliance audits. All documentation linked to specific laboratory equipment asset records.
Internal GMP audit programs, supplier qualification audits, and quality management system reviews. Audit findings and corrective and preventive action plans tracked from identification through verified resolution and effectiveness check.
Pharmaceutical and life sciences operations are subject to comprehensive FDA regulations and international GMP standards that mandate systematic inspection and documentation programs.
Field Eagle maintains timestamped, digitally signed inspection records with complete audit trails. Discuss your specific 21 CFR Part 11 validation requirements with the Field Eagle team to confirm the platform meets your electronic records compliance needs for FDA-regulated operations.
Yes. Field Eagle maintains equipment qualification inspection records linked to specific equipment asset records. IQ, OQ, and PQ inspection documentation, preventive maintenance records, and calibration records are all maintained in the equipment asset history. See: asset management software.
Yes. Field Eagle maintains all GMP inspection records, corrective action documentation, and quality audit histories in one searchable system. Any inspection record is retrievable instantly during an FDA inspection, eliminating the paper file search that commonly consumes FDA inspection time.
