At Validation Resources Group (VRG), our Digital Solution Services division helps medical device manufacturers—and beyond—transition to smarter, validated, paperless systems. We merge regulatory expertise with modern platforms to deliver scalable, GxP-compliant applications.
Digital Integration Initial Assessment
Application Development
CSV Validation & Testing
Quality & Compliance Support
Build interactive, intuitive applications that drive productivity—no coding needed. Use pre-built templates or start from scratch. Manage and govern app development and use on the production floor.
Medical Device
Biotech & Pharma
Regulated Manufacturing
Compliance + Validation Expertise
Strategic SaaS Partnerships
Certified QA & CSV Specialists
At Validation Resources Group (VRG), our Digital Solution Services (DSS) division supports medical device manufacturers and other regulated industries in their transition to smarter, validated, and paperless systems.
We combine deep regulatory knowledge with innovative digital platforms to deliver scalable, compliant, and highly functional applications across the manufacturing and quality lifecycle.
- Digital Integration Initial Assessment
- Evaluate your digital maturity level
- Identify automation opportunities
- Build your roadmap for smart manufacturing
- Build no-code / low-code apps on Tulip, etc
- ERP & equipment connectivity
- UI/UX design tailored to operators
- Full Computer System Validation lifecycle (GxP)
- Documentation with traceability matrices (Tulip)
- Testing protocols (IQ, OQ, PQ)
- Digital CAPA and NC workflows
- eLogbook implementation
- QA dashboards and KPI reporting
We work with trusted platforms to deliver results: Tulip Interfaces – No-code apps, eDHR, eLogbooks
eDHR (Electronic Device History Record)
- Paperless manufacturing records
- Real-time data capture and approvals
- ERP and equipment integration
- Digital logs with timestamp and audit trail
- Replace paper-based GMP logbooks
- Configurable workflows
- Structured QA workflows
- Dashboards for monitoring and reporting
- Integrated with QMS or as standalone
- Medical Devices
- Pharmaceutical & Biotech
- Food & Beverage
- Regulated Manufacturing
- 20+ years of industry compliance expertise
- Strategic partnerships with best-in-class platforms
- Certified professionals in CSV, QA, UI/UX, and validation
- Deep experience in GxP, FDA, and ISO standards