LabSync Group Consultancy configures, qualifies, and connects your LIMS — end to end. LIMS v3 & v4 specialists serving global pharmaceutical clients.
LabSync Group Consultancy was founded by LIMS practitioners who built and qualified laboratory systems in pharmaceutical environments for over a decade. We've sat in the labs we now configure.
Our team specializes in LIMS Versions 3 and 4, covering every module, every spec, and every compliance requirement — for pharma clients across India, US, and Europe.
Every service is delivered by consultants with real lab experience — not just certification.
Complete master config across all modules — every spec type from raw material through finished product, all the way to Test Plan level.
Sample Manager · Resource ManagerEverything required to register your lab site — users, roles, instruments, departments — so go-live has no gaps.
Site Onboarding · Role ConfigBidirectional integration between instruments and LIMS. Interface mapping, driver config, validation, and documentation.
Interface · ValidationERP, MES, and third-party integrations — API design, middleware config, and end-to-end testing in regulated environments.
ERP · SAP · MESProtocol authoring to test execution — complete, audit-ready PQ packages aligned to your regulatory framework.
PQ Protocol · Deviation MgmtGMP SOPs, PQ scripts, and validation documentation — tailored to your LIMS version and ready for regulatory submission.
GMP SOPs · ScriptsFull project scope from kickoff to handover — requirements, masters, integration, qualification, training, and stabilization.
Full Scope · Project MgmtRole-based training for end users, super users, and administrators — with documentation to support long-term self-sufficiency.
Role-Based · AdminOngoing troubleshooting, change requests, master updates, and periodic system reviews after launch.
Support · Change RequestsDeep hands-on expertise across both LIMS generations — covering migration paths, module nuances, and version-specific validation requirements.
Product types, specifications, methods, and sampling plans — fully configured within the Sample Manager module.
Instrument records, reagents, stability scheduling, and resource lifecycle configuration.
All spec types through Test Plan level — with limit sets, result entry forms, and approval routing.
Stability study setup, time-point scheduling, pull list generation, and results tracking.
Electronic routing, multi-level approval chains, and e-signature setup — 21 CFR Part 11 aligned.
Migration planning, master re-mapping, gap analysis, and requalification support when upgrading versions.
Certificate of Analysis templates, custom reports, and label configuration for GMP and commercial needs.
Configuration and troubleshooting of supplementary LIMS tools and master data management utilities.
Every deliverable is authored with compliance baked in — masters, protocols, SOPs, and scripts.
Our engagement model is built for regulated environments — where scope clarity and documentation are non-negotiable. Every project follows a defined, auditable path.
Audit current setup, identify gaps, align on scope, timelines, and deliverables before any configuration begins.
Systematic creation across all modules — with QA-approved checkpoints at each phase.
Instrument interfaces configured and tested. ERP/MES integrations validated in your environment.
Protocol authoring, test execution, deviation resolution, and audit-ready documentation package.
Role-based training delivered. SOPs handed over. Your team self-sufficient before we close the project.
Every consultant has direct pharmaceutical laboratory experience — not just system training.
Tell us about your LIMS project — we'll respond within one business day to schedule a focused technical discussion or live demo.
contact@labsyncgroup.com
+91 79850 74374 (Sales)
India · USA · Europe · Global
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