Adris Pharma Services
Your Trusted Partner in Remote Pharmaceutical Engineering & Systems compliance
GMP | Risk Assessment | Streamlined IOPQ
Adris
Pharma Services - at a glance
Remote Validation Expertise. Risk-Based Precision. GMP Compliance Delivered.
Adris Pharma Services is a remote-first pharmaceutical consultancy specializing in GMP compliance and remediation, risk-based validation, and computerized systems validation (CSV). The consultancy empower pharmaceutical companies with scalable, cost-effective solutions that ensure audit readiness and operational excellence—without compromising quality. Using an iterative, risk-based approach aligned with GAMP 5 and 21 CFR Part 11 standards, Adris Pharma Services supports validation across facilities, equipment, utilities, and computerized systems.
Discover the story behind Adris Pharma Services
core SErvices overview
Smarter Validation & Compliance for Pharma Manufacturing
Adris Pharma Services is an independent, remote-first consultancy that helps pharmaceutical manufacturers go beyond compliance—turning it into a strategic advantage.
The consultancy provides specialized CQV and CSV expertise without the overhead of full-time, on-site teams. The result: faster timelines, reduced costs, and seamless collaboration with internal quality, engineering, and regulatory teams.
Adris Pharma Services focuses on what matters most: risk-based validation, GMP gap remediation, and inspection-ready documentation. From IQ/OQ/PQ protocol development and computerized systems validation to SOP development lifecycle documentation, the consultancy brings clarity, agility, and confidence to every step.
Partner with Adris Pharma Services—where compliance meets confidence, and operations move forward with purpose.
Why Adris Pharma SErvices?
Remote-first model that reduces cost, not quality
Deep expertise in pharma manufacturing compliance
Agile, risk-based validation tailored to your needs