Release faster without compromising compliance
Scriptless test automation across connected LIMS, MES, SAP, and eQMS, with timestamped, ALCOA+ evidence.
No-code test automation for pharma validation
Testing gaps in pharma don’t stay small. They turn into missed timelines, lost revenue, and regulatory findings.
of clinical trials miss their Initlal timelines
Tufts CSDD, 2024
of FY25 FDA warning letters cite data integrity issues
Tufts CSDD, 2024
rise In FDA drug warning letters, FY24 -> FY25
Pharmaceutical Online
Our portfolio of pharma testing services
From clinical trials to manufacturing, we test every GxP system in your stack and the integrations that link them.

Risk assessment
Classify by intended use - every function scored for business critical risk assessment before any testing begins.
Test strategy
We don't test everything the same way. Each function gets tested based on how much risk it carries.
Automate
Reusable test suites - build once, adapt automatically as your applications change.
Validate & qualify
IQ/OQ/PQ, E2E - formal qualification and end-to-end testing for what genuinely needs it.
Evidence & maintain
ALCOA+ records - attributable, legible, contemporaneous, and complete documentation, maintained continuously.
Why pharma companies choose Sedstart
Sedstart combines no-code automation with deep pharma expertise, so your team gets validation that fits your systems, spans your whole workflow, and stands up in an audit.

How Life Sciences protected $2M in revenue
Sedstart transformed legacy application testing by pairing requirement-based load testing with custom test automation, helping a global clinical research leader eliminate performance bottlenecks and achieve audit-ready compliance instantly.
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0 New hires needed
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20 Modules load-tested
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100+ Functional test cases automated
Hear from engineering leaders who’ve transformed their testing with Sedstart’s no-code automation tool.
Your queries, our answers
What makes pharma testing different from other industries?
Can you test our custom-built pharma applications alongside SAP?
How do you ensure FDA 21 CFR Part 11 compliance in testing?
Do you support clinical trial management system testing?
Can you work with our existing QA and compliance teams?
How quickly can you set up automated testing for our pharma systems?
What kind of compliance documentation do you provide?
Does Sedstart handle IQ/OQ/PQ qualification testing?
















