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 consulting firm specializing in GMP compliance, risk-based validation, and computerized systems validation (CSV). We empower pharmaceutical companies with scalable, cost-effective solutions that ensure audit readiness and operational excellence—without compromising quality. Our iterative, risk-based approach supports validation across facilities, equipment, utilities, and systems, aligning with GAMP 5 and 21 CFR Part 11 standards.
Discover the story behind Adris Pharma Services
core SErvices overview
Smarter Validation & Compliance for Pharma Manufacturing
At Adris Pharma Services, we don’t just support compliance—we help you lead with it. Our remote-first model empowers pharmaceutical manufacturers to access specialized CQV and CSV expertise without the overhead of full-time, on-site teams. The result? Faster timelines, reduced costs, and seamless collaboration with your internal quality, engineering, and regulatory teams.
We focus on what matters most: risk-based validation, GMP gap remediation, and inspection-ready documentation. From IQ/OQ/PQ and computerized systems validation protocol development to SOP development and lifecycle documentation, we bring clarity, agility, and confidence to every step.
Partner with Adris Pharma Services—where compliance meets confidence, and your 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