Compliance Made Simple. Flexibility Built In. 

In today’s Life Sciences landscape, compliance isn’t just a requirement it’s a strategic priority. But legacy quality systems are often rigid, fragmented, and slow your teams down. At Simploud, we believe quality shouldn’t come at the cost of agility. 

Simploud is a modern, cloud-based compliance platform purpose built for regulated industries pharmaceutical, biotech, medtech, laboratories, clinical research and all related Suppliers. Designed for compliance and engineered for flexibility, our platform helps you meet global GxP requirements with ease, speed, and confidence. 

Why Simploud 

Simploud aligns with 21 CFR Part 11, Annex 11, GAMP 5, and ISO 9001/13485/14971/27001. Built-in validation, audit trails, electronic signatures, and traceability make inspection-readiness the default – not a scramble. 
From Document Control and CAPA to Training, Audits, LIMS, Risk, Supplier Management, etc., you get the modules you need configured to your workflow without writing a line of code. 
Deployed in weeks, not months. Hosted securely on the Salesforce Lightning Platform with regional hosting options (EU, U.S., APAC). Scalable from preclinical to commercial stage.
Track Critical-to-Quality (CtQ) factors, KPIs, KRIs, and Quality Tolerance Limits (QTLs) across your organization and supplier base so you see issues before they become risks.
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Trusted by Life Sciences Leaders Worldwide 

Simploud supports innovators across clinical and commercial pipelines from VC-backed biotechs to global medtech firms. Customers choose us for our compliance depth, intuitive design, and ability to scale alongside their growth. 
Whether you’re preparing for your first regulatory submission or managing a global portfolio, Simploud helps you turn quality from a checkbox into a competitive advantage. 
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