Mission
Bring quality under clearer control
Complere helps teams replace fragmented quality operations with connected workflows, stronger traceability, and more confident oversight across every inspection-ready process.
Company
Built by life sciences SaaS veterans
Founded by Scilife alumni. 30+ years combined inside regulated quality software, building for pharma, medical device, and biotech quality teams.
Complere helps pharmaceutical, medical device, and life sciences organizations replace fragmented quality operations with connected, inspection-ready workflows — making compliance a daily operating practice, not just an inspection preparation task. We build for ISO 13485–style rigor in device settings and GxP scrutiny in pharma — with risk-based quality management as a through-line, not a slide deck afterthought.
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30+ yrsCombined life sciences SaaS experience
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200+Clients shipped to in prior roles
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20K+Users supported at scale
What we help teams change
We work with organizations moving away from paper, spreadsheets, and hard-to-adopt legacy systems. The goal is not only digitization, but clearer ownership, stronger retrieval, and better leadership visibility.
- Document governance
- CAPA and deviation control
- Audit readiness
- Management review visibility
Why Choose Complere
Built for regulated life-sciences teams that need control, auditability, and practical adoption.
Approach
Designed for compliance and practical adoption
The platform is built for real-world regulated rollout — electronic signatures, validation-ready documentation, and phased deployment are features, not optional extras.
Focus
Purpose-built for regulated life sciences
Our platform is tuned for the specific workflows, compliance frameworks, and inspection expectations of pharmaceutical, biotech, medical device, and adjacent markets.
Meet the founders
Built by people who have done this work
30+ years combined inside life sciences SaaS at Scilife and elsewhere. We did not set out to build software. We set out to fix what we kept running into: tools that were expensive to license, painful to validate, difficult to adopt, and built for compliance theatre rather than real operating practice.
Founder
Jitendra (Jatin) Dhoot
Founder, Complere
20+ years across IT and entrepreneurship, 10+ in life sciences software. Built Scilife India from one person to a 35+ member team. Focused on systems that surface quality risk before it becomes audit findings.
Ex-Scilife
20+ yrs IT
Co-founder
Abdul Karim
Software Architect & Infrastructure Lead
10+ years building reliable, audit-ready systems for life sciences SaaS. Designed Complere's multi-tenant architecture, tenant isolation, access control, and audit trail integrity from day one.
Ex-Scilife
10+ yrs SaaS
Co-founder
Vijay Kumar
Validation & Engineering · DevOps Lead
10+ years in life sciences software. Prepares both CSA and CSV validation suites end-to-end across every module — URS, RA, CS, TP, TM, IQ/OQ, PQ, TSR/VSR.
Ex-Scilife
CSA & CSV ready
How we think about rollout
Complere favors phased adoption. Teams can start with a focused pilot, prove fit in one workflow, and expand once the operating model is stable and validated.
- 30-day pilot option
- Configurable per industry
- CSV validation package included
Ready to see how Complere can work for your team?
Start with a focused demo, a 30-day pilot, or just a conversation about your quality priorities.