Is Your Cleaning Validation Process Becoming a Challenge?
Paper records, manual entries, multiple approvals, difficult traceability and time-consuming audit preparation can make an essential process harder to control.
01
Manual RecordsPaper & spreadsheets02
Data EntryRepetitive manual work03
ReviewSlow verification04
ApprovalManual routing05
TraceabilityRecords hard to find06
AuditTime-consuming preparationWhat if your entire cleaning validation journey could be controlled digitally?
Digital Execution
Guide cleaning activities through structured digital workflows, tasks and approvals.
Controlled Data Capture
Capture cleaning parameters, observations and validation evidence in a structured digital environment.
Workflow Automation
Automate tasks, approvals and notifications to reduce repetitive manual effort.
Data Integrity & Traceability
Maintain electronic records, secure audit trails and complete cleaning history.
Compliance Management
Support regulated workflows, electronic signatures, approvals and audit readiness.
Analytics & Visibility
Turn validation information into dashboards, reports and actionable insights.
FROM MANUAL TO DIGITAL
Upgrade the Process - Not Just the Paper
Digital transformation should not mean simply replacing a paper form with an electronic form. RadiantPRO helps transform how cleaning activities are executed, controlled, documented, reviewed and managed.
TRADITIONAL / MANUAL
Paper-based checklists and records
Manual recording and transcription
Paper routing and manual signatures
Scattered historical records
Manual report preparation
Manual review and record collection
Limited status visibility
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RADIANTPRO
Digital cleaning workflows and records
Structured digital data capture
Configurable workflow and electronic signatures
Centralized cleaning history and audit trail
Standardized digital reports
Controlled, traceable digital process
Digital status, analytics and insights
RADIANTPRO DIGITAL JOURNEY
Cleaning Validation Lifecycle
A connected digital journey designed to standardize validation activities, strengthen compliance and provide greater visibility across the cleaning validation lifecycle.
1
Validation Planning
Plan and standardize validation activities within a controlled digital environment.
2
Digital Execution
Guide activities through structured digital workflows, tasks and approvals.
3
Verification
Capture validation evidence and support systematic verification of cleaning activities.
4
Compliance Insights
Transform validation information into actionable visibility, analytics and audit-ready insights.
5
Ready for Production
Support controlled equipment readiness while maintaining traceability and compliance.
WHAT DO YOU GAIN?
Better Quality. Greater Efficiency. Stronger Compliance.
RadiantPRO delivers value across quality, compliance and operations by digitizing and standardizing the cleaning validation lifecycle.
01
Better Compliance
Maintain controlled records, audit trails, electronic signatures and traceability to support regulated operations.
02
Higher Data Integrity
Reduce risks associated with manual transcription, incomplete records and disconnected information.
03
Faster Operations
Reduce paperwork, repetitive documentation and manual review activities.
04
Consistent Processes
Standardize cleaning execution and validation practices across equipment, production areas and sites.
05
Complete Visibility
Gain visibility into cleaning status, history, validation information and compliance activities.
06
Enterprise Scalability
Support a common digital cleaning validation platform across multiple plants and locations.
COMPLIANCE
Built for Global Regulatory Compliance
RadiantPRO is designed to help organizations meet stringent regulatory expectations and maintain audit readiness across the enterprise.
FDA21 CFR
Part 11
Part 11
FDA 21 CFR Part 11
Designed to support electronic records, electronic signatures and closed-system requirements.
EUGMP
Annex 11
Annex 11
EU GMP Annex 11
Supports computerized systems in regulated environments in alignment with Annex 11 expectations.
ALCOA+
ALCOA+ Principles
Supports data integrity principles including attributable, legible, contemporaneous, original, accurate and complete records.
GAMP5
GAMP 5 Aligned
Built in alignment with GAMP 5 principles for validated, reliable and compliant computerized systems.
cGMP
cGMP Aligned
Supports current Good Manufacturing Practice expectations for quality, consistency, traceability and patient safety.
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Compliance by Design. Confidence by Default.
RadiantPRO® helps organizations remain inspection-ready through secure, controlled and traceable digital processes.
ENTERPRISE CONNECTIVITY
Connected to Your Enterprise Ecosystem
RadiantPRO can integrate with enterprise systems and instruments to create a unified, connected digital ecosystem.
RadiantPro®Cleaning Validation &
Compliance Platform
Compliance Platform
LIMS
Laboratory data and results integration
QMS
Quality events, CAPA and change-control integration
ERP
Material, organizational and enterprise data integration
MES
Manufacturing execution and production data integration
Data Sources
Connect relevant digital data sources and instruments
Enterprise Systems
Support a connected manufacturing and quality ecosystem
Don't Just Digitize the Documents. Transform the Process.
Digital transformation does not have to mean completely redesigning your cleaning process. Anmeda will work with you to understand your current process, identify opportunities for improvement and develop the right digitalization approach for your organization.
