Pharma
How do you protect your research and prove compliance while keeping production moving?
Pharma companies hold valuable formulations, trial data and validated manufacturing records. Regulators and customers expect access control, audit trails and documented change management.
Strong data protection and inspection-ready records keep both your intellectual property and your licences safe.
So why shouldn’t your IT services reflect that?
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Why not see how ISS Technologies can support your Pharma business?
Explore Our ServicesChallenges we help solve
Pharma companies protect formulations, trial data and validated manufacturing systems. We secure IP and regulated records, keep plant and corporate IT running and help teams stay inspection-ready.
Intellectual property theft
Formulations, R&D data and trial results are valuable targets for attackers and competitors.
Data integrity expectations
Regulated records need access control, audit trails and tamper-evident storage.
Validated systems
Changes to systems in regulated environments must be controlled and documented.
Plant and corporate IT together
Manufacturing, labs and enterprise IT share networks and need clear segmentation.
How ISS Technologies helps
Services we typically bring to Pharma organisations.
Data Loss Prevention
Control how R&D and regulated data is shared, copied and emailed.
Compliance
Support data integrity, audit trails and inspection readiness.
Managed SOC
Monitor corporate, lab and plant-adjacent networks continuously.
Cybersecurity (VAPT)
Test applications and infrastructure that handle regulated data.
Patch & Vulnerability Management
Planned, documented patching that respects validation requirements.
Microsoft 365
Secure collaboration with sensitivity labels and controlled sharing.
Frameworks and regulations we work with
We confirm which regulations apply to you during the first consultation.
Technical controls we typically put in place
- Data integrity (ALCOA+)Audit trails, access controls and change control on GxP systems.
- Validated environmentsDocumented change and patch process that keeps validated systems in a known state.
- IP protectionDLP, encryption and access control for R&D and formulation data.
- Plant and corporate ITSegmentation and monitoring across manufacturing and corporate networks.
How an engagement runs
A simple, repeatable path from first review to steady operations.
Classify
Identify IP and regulated data and decide how each type is handled.
Control
Apply access, DLP and change controls that fit validated environments.
Monitor
Watch for unusual access, copying or outbound transfers.
Prove
Keep logs and reports ready for inspections and customer audits.