Two pillars, one partner
Expert pharmaceutical consulting, powered by practical digital solutions.
Many firms offer consulting. Many sell software. Very few combine both. ValPro delivers science-based consulting and the digital tools that put the same rigor directly in your hands.
Industry Experience
15+ years inside real GMP facilities — protocols written and inspections survived, not theorized
Global
Compliance
Compliance
FDA, EU GMP, MHRA, and regional authorities — one partner fluent across your target markets..
Digital Innovation
Excel toolkits, SaaS platforms, and AI compliance assistants built from real validation practice.
Practical
Solutions
Solutions
Implementation that works on the floor and survives an audit — strong documentation, every time.
- Pillar 1 · Consulting Services
Expertise across the full GMP lifecycle
From quality systems to validation, sterility, and inspection readiness — scoped, delivered, and documented to satisfy global regulators.
Quality Assurance
QA systems, oversight, and continuous compliance.
Validation & Qualification
Process, equipment, facility & utilities, CSV.
Sterility Assurance
Aseptic processing and microbial control.
Annex 1 & CCS
Contamination Control Strategy aligned to Annex 1.
Quality Management Systems
QMS design, gap assessment, remediation.
Inspection Readiness
Mock inspections and pre-audit gap closure.
Technical Documentation
Protocols, reports, and SOP development.
Training Programs
GMP, data integrity, and role-based training.
Computer System Validation
CSV and 21 CFR Part 11 / Annex 11 compliance.
- Why Clients Choose Us
A risk-based, practical approach — built to pass.
We don't deliver theory. We deliver protocols, systems, and documentation that work on the floor and stand up to FDA and EU GMP scrutiny.
✓ Regulatory alignment — fluent across FDA, EU GMP, MHRA & regional bodies.
✓ Practical implementation — solutions your team can actually run.
✓ Strong documentation — audit-ready files, every engagement.
✓ Digital-first mindset — tools that make compliance repeatable.
- Pillar 2 · Digital Solutions
The expertise, productized
We build the tools our own consultants use — from free calculators to professional Excel toolkits, and a growing cloud platform with AI compliance support.
Available
Free & Professional Tools
Validation Matrix, Sampling Calculator, Project Planner — plus professional Excel toolkits: VMP Builder, Equipment Qualification Tracker, Cleaning Validation Calculator, Inspection Readiness Checklist.
Emerging
Cloud SaaS Platform
Inspection Readiness, CAPA Management, Validation Lifecycle Management, and Risk Assessment — moving your compliance workflows off spreadsheets and into a secure platform.
In Development
AI Compliance Assistant
'An AI assistant that drafts protocols, checks documents against regulations, and answers GMP questions — always with a human in the loop.
- Industries We Serve
Built for regulated life-science manufacturing
Sterile Manufacturing
Aseptic fill-finish, Annex 1, and contamination control.
Oral Solid Dosage & Liquids
Process validation and equipment qualification.
Biotechnology
Biologics, cell & gene therapy quality systems.
Medical Devices
ISO 13485 and combination-product compliance.
Laboratories
Data integrity, CSV, and analytical compliance.
CDMOs & Healthcare
Multi-client readiness and quality oversight.
- Trusted by pharmaceutical professionals
Built on real industry credibility
Representative of the engagements we support · Named client stories coming soon
- Knowledge Center
GMP insights & validation guides
Practical guidance on Annex 1, FDA & MHRA inspections, validation, and QMS best practice.
What Annex 1 changed for your CCS
The revised Annex 1 reframes contamination control as a strategy. Where to start.
The five gaps inspectors find first
Most 483 observations cluster in a handful of predictable areas.
Making ALCOA+ practical
Data integrity fails in the day-to-day. A practical way to operationalise it.
Let's strengthen your compliance — and your confidence.
Practical guidance on Annex 1, FDA & MHRA inspections, validation, and QMS best practice.
Representative of the engagements we support · Named client stories coming soon