Healthcare & Pharma
GMP, GLP, and ISO 15189 — compliance automated.
Compliance and patient safety, automated. From batch records to lab competency, every step is traceable and auditor-ready.
Day 1
audit readiness — GMP, GLP, and ISO 15189 templates pre-loaded
Per shift
training competency tracked per role, per worker — no spreadsheets
Sealed
batch records and lab QC available to inspectors in one secure link
The hidden tax on healthcare SMEs.
Batch records that can't be retrieved fast enough. Training competency that lives in spreadsheets. Inspections that find issues nobody could see in time to fix them.
How Radqal solves it.
- GMP, GLP, and ISO 15189 templates pre-loaded and version-controlled.
- SMS-based deviation logging and AI-suggested CAPAs.
- Training competency tracked per role, per worker, per shift.
- Blockchain-sealed batch records and lab QC for instant inspector access.
Validation Protocols
How Radqal validates your compliance.
Step-by-step AI-guided checklists for every standard your buyers and auditors require — pre-configured and ready from day one.
GMP
- 1Batch manufacturing records completed per production run — deviations flagged in real time and closed with CAPA
- 2Equipment cleaning and maintenance logs captured per validated schedule via SMS or app
- 3Training competency records verified per role, per shift — knowledge gaps auto-linked to CAPA and remediation
- 4Finished product release checklist completed and records sealed for regulatory inspector access
GLP
- 1Study director and study plan documented and version-controlled before experimental work begins
- 2Raw data captured with audit-trail timestamps — instrument readings logged at source, not retrospectively
- 3Deviation and amendment records linked directly to the affected study phase and sample batch
- 4Archive-ready final study report with complete audit trail sealed to blockchain for regulatory submission
ISO 15189
- 1Laboratory scope, examination procedures, and staff competency requirements version-controlled and accessible
- 2Equipment calibration and maintenance records verified against manufacturer criteria and accreditation schedule
- 3Internal quality control and external quality assessment participation records linked to individual competency data
- 4Non-conforming examination results logged immediately — AI triggers clinical review and CAPA automatically
Related Resources
Quality Masterclass
Six weeks to quality excellence — live cohort sessions with your industry peers every Thursday.
Enrol free →NewsletterThe Qualimetrique
Twice-monthly quality insights for African SME owners — standards made simple, no jargon.
Subscribe free →PlatformRadqal Platform
Six integrated modules — CAPA, audits, training, traceability, documents, and reporting.
Explore the platform →Case story.
A Ghanaian diagnostic lab adopted Radqal for ISO 15189 readiness. They closed 22 non-conformities in 6 weeks and passed accreditation on first attempt.