Template

GMP SOP Audit for Tablet HSC and Softgel

by Gary Callahan, from the Community

Conduct a thorough GMP SOP audit across tablet, hard shell capsule, and softgel operations. This checklist references 21 CFR 111 and related FDA standards and covers facility and grounds, receiving and quarantine, warehouse storage, weighing, blending and compounding, tablet pressing and coating, hard shell and softgel encapsulation, packaging and powder filling, maintenance, quality control laboratory, quality assurance, documentation, training, vendor qualification, investigations, and sample retention. Use it to score compliance and capture auditor and company sign off.

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Digitize any process, procedure or policy

Eliminate mistakes made by paper-based processes

Create and share professional reports instantly

Confirm accountability and compliance with a digital log

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This community page makes available free workplace checklists and templates created by other users within the SafetyCulture community. SafetyCulture has re-published this content and where possible, has credited the original author. SafetyCulture has not verified the accuracy, reliability or suitability of any community content. You agree that your use of any of this content is in accordance with SafetyCulture’s Terms and Conditions.

Template
GMP/SOP Audit for Tablet and HSC Manufacturing
This comprehensive GMP and SOP audit checklist supports tablet and hard shell capsule manufacturing operations in meeting 21 CFR 111 requirements. It covers receiving, warehousing, weighing, blending and compounding, tablet compression, coating, encapsulation, packaging, quality control laboratory, and quality assurance. Use it to verify documentation, calibration, sanitation, training, investigations, and vendor qualification, helping teams find gaps and improve compliance and product quality.
by Gary Callahan, from the Community
Downloads: 10+
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Template
GMP and SOP Audit Checklist for Softgel Manufacturing
This GMP SOP audit checklist supports softgel manufacturers in meeting FDA 21 CFR 111 requirements for dietary supplements. Use it to review facility hygiene, pest control, receiving, quarantine, warehousing, weighing, blending, encapsulation, polishing, inspection, packaging, and general housekeeping. Verify calibration and maintenance, documentation, batch and master records, vendor qualification, training, investigations, quality control lab practices, and quality assurance procedures to drive compliance and product quality.
by Gary Callahan, from the Community
Downloads: 10+
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Template
GMP/SOP Audit Checklist for 21 CFR 111
This GMP and SOP audit checklist helps manufacturers evaluate compliance with 21 CFR 111 for dietary supplements. It covers facility and grounds, receiving and quarantine, warehouse controls, weighing, blending and compounding, hard shell encapsulation and polish/inspect, packaging and powder filling, maintenance, quality control laboratory, quality assurance, documentation, and training records. Prompts reference applicable FDA requirements, verify SOPs and calibration logs, and guide investigations and vendor qualifications. Ideal for pharmaceutical and supplement operations seeking structured GMP audits and clear scoring thresholds.
by Gary Callahan, from the Community
Downloads: 10+
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Template
GMP SOP Audit for Softgel Manufacturing
This GMP SOP audit checklist is designed for softgel manufacturing and dietary supplement facilities. It guides auditors through facility and grounds, receiving, warehouse, weighing, blending, encapsulation, polishing and inspection, packaging, maintenance, quality control laboratory, quality assurance, and documentation. Checks cover sanitation, pest control, equipment identification and calibration, gowning, labeling, in process controls, record keeping, vendor qualification, investigations, and training. Use it to benchmark operations against FDA 21 CFR 111 requirements and capture notes, evidence, and signatures. The scoring approach supports percentage based compliance evaluation, with typical qualification at 90 percent and a minimum of 85 percent based on severity.
by Gary Callahan, from the Community
Downloads: 30+
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GMP SOP Audit for Tablet HSC and Softgel

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