Confidence Built on Compliance
We don’t just follow standards. We design pharmaceutical compliant software and systems that lead them
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In cleanroom and regulated environments, compliance isn’t an afterthought, it’s the foundation.
Our pharmaceutical compliant software is designed to support data integrity, audit trails, and long-term traceability in GMP-regulated environments. Every product, service, and support process is shaped around the regulations that matter to you.
We build for audit trails. We design for data integrity. And we support you with documentation that stands up to inspection, every time.
Meet Your QHSE Team
Your compliance journey is only as strong as the people behind it. Our dedicated Quality team works hand-in-hand with your stakeholders and regulators to ensure that every system is audit-ready, from the first installation to your final inspection.
Certifications & Supporting Documents
Our pharmaceutical compliance software doesn’t just meet industry standards, it is backed by the documentation to prove it. Below you’ll find our key certifications and compliance statements, ready for audits, procurement processes, and quality reviews. If you need something specific, our Quality team is here to help.
Quality
Quality isn’t just a box we tick; it’s embedded in every part of how we work. From product development to installation and support, our internal procedures are designed to meet the strictest regulatory requirements and deliver complete confidence in our systems. Learn more about us.
Sustainability
Sustainability is more than a policy; it’s a responsibility we take seriously. We are committed to reducing environmental impact, preventing pollution, and protecting the environments we operate in.
Through our Environmental Management System, we set clear objectives to drive continuous improvement and align with ISO 14001:2015 standards. We work to meet, and where possible, exceed, all relevant environmental legislation and compliance obligations.
Accreditations
Our accreditations reflect our commitment to industry-leading standards and continuous improvement across everything we do. If you need anything further, our Quality team is here to help.
ISO 9001:2015
Certificate Reference:
FS 621150
Scope:
Design, supply, implementation,
and maintenance of
environmental and particle
monitoring systems.
Initial accreditation:
06-February-2017
Expiry:
01-February-2026
ISO14001:2015
Certificate Reference:
EMS 798612
Scope:
Design, supply, implementation,
and maintenance of
environmental and particle
monitoring systems.
Initial accreditation:
12-March-2025
Expiry:
11-March-2028
ISO 17025:2017
Calibration Laboratory No:
24752
Initial accreditation:
15-September-2022
Expiry:
Re-certification audit is annual.
To see the scope of our accreditation, please click the link below
Additional Download(s)
Schedule of Accreditation
Cyber Essentials
Certificate Reference:
937b1d37-4b02-4af0-8305-86a259d6f8e3
Initial accreditation:
30-May-2022
Expiry:
15-July-2025
Safe Contractor
Certificate Reference:
MU2560
Initial accreditation:
20-February-2016
Expiry:
14-March-2026
Additional Download(s)
Certificate of Verification
Constructionline
Certificate Reference:
162176
Initial accreditation:
November 2015
Expiry:
12-May-2026
Pharmagraph’s validation documents passed our audit with zero observations. Their attention to compliance saved us time and gave us total confidence."
QA Lead, Biotech Manufacturing Facility
Who We Are. What We Deliver.
From decades of industry experience to the systems we build today, everything we do is grounded in compliance, performance, and trust. Join us behind the scenes of world-class pharmaceutical monitoring, and help shape the solutions that keep our partners ahead.
Accreditations & Assurance
Our pharmaceutical compliance software meets the latest regulatory expectations, including 21 CFR Part 11 and GAMP 5. We build confidence into every system, but we back it with proof.
