Enabling lifesciences industry to thrive

Empowering teams. Aligning operations. Enabling transformation.

At Liorta, functional advisory isn’t just about process documentation – it’s about unlocking domain excellence across borders and roles. We specialize in bi-lingual (English & Japanese), regulatory-first training and functional support tailored specifically for life sciences, pharmaceutical, and biopharma enterprises.

From onboarding new tools to optimizing existing workflows, our advisory services ensure your teams are prepared, aligned, and empowered to drive performance across regions. We conduct in-depth fit-gap analysis to guide vendor/product selection and help your internal teams evolve into functional experts through curated enablement tracks.

Whether you’re fine-tuning pharmacovigilance processes or preparing for compliance rollouts, our advisors combine global regulatory understanding with on-ground operational insight. Combined with our business process optimization models and third-party evaluation frameworks, you gain a powerful, end-to-end toolkit designed to drive sustainable and functional success.

• Domain-centric, real-world aligned training
• Business workflow improvements and SOP alignment
• Regulatory advisory built into every recommendation
• Functional expert enablement across global teams
• Vendor evaluations & product fit-gap strategy

The result? Trained people. Better processes. Smarter decisions.

Because at Liorta, we don’t just train — we transform capability into competitive edge.

From vision to execution — with regulatory precision.

Liorta’s consulting and implementation services bring deep life sciences expertise and structured delivery methodologies to every engagement. Whether you’re upgrading systems like Drug Safety, Regulatory, or Quality, transforming end-to-end business processes, or navigating post-merger integrations – we are your trusted partners in driving regulated change.

We begin with thorough alignment workshops and discovery sessions, followed by iterative design, modeling, and validation cycles. Our team ensures that each configuration and customization meets regulatory requirements while optimizing for performance and scale. We support multiple systems – from Argus and ArisGlobal to IQVIA and Veeva platforms – with an emphasis on future-readiness.

M&A? We’ve got it covered. Our team supports organizational transitions with data migration, analytics, and signaling intelligence that ensure business continuity and compliance across new structures. With predefined accelerators, reusable scripts, and validation artifacts, we help you save time, reduce cost, and eliminate friction.

• Regulatory updates & business rule customizations
• Process reengineering for compliance and efficiency
• Implementation, configuration, and validation
• Data migration & systems integration
• Analytics, dashboards & post-go-live support
• M&A and divestment solutioning

We don’t just consult. We co-create, implement, and deliver results.

Because real transformation demands both expertise and execution.

Always-on. Scalable. Regulatory-ready.

Liorta’s Enterprise Support services are built to ensure your mission-critical life sciences operations remain compliant, resilient, and efficient — around the clock.

Our expert teams integrate directly into your workflows, delivering end-to-end technical and functional support — from real-time issue resolution to proactive system enhancements. Choose from 24/7 or 24/5 support models, tailored to your business needs, for uninterrupted service coverage across time zones.

We maintain consistent uptime and business continuity across global infrastructures by managing updates, user provisioning, configurations, and data integrity. With bilingual (English–Japanese) capabilities and real-time dashboards, we connect seamlessly across teams, geographies, and functions.

Our support offering includes:

• Functional, technical, and infrastructure-level support
• User onboarding and business configuration updates
• Reporting and operational assistance
• Patch and change management aligned with regulatory requirements
• Real-time application, database, and scheduler monitoring
• Early-late case detection and compliance alerting

Our support goes beyond stability — we help evolve your enterprise stack for long-term agility and compliance.

Talk to our experts about building a reliable, future-ready support backbone.

Always-on, compliance-first, and worry-free support.

Liorta’s Managed Services go beyond traditional IT support — we provide a comprehensive operational ecosystem purpose-built for regulated life sciences businesses. Our global-tiered support model (L1–L3) combines domain understanding, functional expertise, and technical precision. Add 24/7 coverage and bilingual (English–Japanese) capabilities, and you get global scale with local fluency.

From managing user maintenance requests to resolving backend challenges like integration failures and patch deployments, our teams embed directly into your workflows. We continuously monitor applications, databases, and scheduler logs using real-time dashboards — enabling early detection of potential disruptions (like processing delays or failed submissions) and timely escalations of sensitive cases that could affect compliance timelines.

We collaborate closely with your internal stakeholders, product vendors, and cloud partners to create a unified support experience. Our Operational Governance Framework ensures transparency and accountability through compliance trackers, SLA dashboards, RCA/CAPA workflows, and structured knowledge repositories.

Our support covers:

• End-to-end support: Functional, technical, and infrastructure
• Patch & change management within regulatory frameworks
• Real-time monitoring, alerts, and proactive resolution
• User onboarding, business configuration, and reporting assistance
• Compliance oversight with SLA metrics, RCA/CAPA, and audit readiness
• Tiered bilingual support models (12/5 to 24/7)

With Liorta, your systems don’t just stay operational — they’re continuously optimized for what’s next.

You focus on growth. We handle the rest.

Domain-first development. Built for the regulated enterprise.

In a world where generic solutions fall short, Liorta builds tailored technologies designed specifically for the life sciences industry. Our development services are not just about writing code – they’re about solving problems that demand domain intelligence, compliance knowledge, and technical innovation.

From configuring business-specific applications to crafting custom reports, integrations, and ETL pipelines – we bring workflow-aligned, agile engineering to your doorstep. Our solutions drive automation, reduce manual overhead, and enable real-time visibility across safety, regulatory, and quality operations.

But we don’t stop at operational tooling. We engineer AI-augmented platforms that generate predictive insights, optimize decisions, and enhance performance across your value chain. Whether you need an automated reconciliation tool, an intelligent reporting system, or a bespoke compliance dashboard – we build it with purpose.

• Application customizations for life sciences workflows
• Automated tools, bots & micro-platforms
• Advanced analytics, dashboards, and ETL pipelines
• AI/ML-led solutions for decision-making & insights
• Agile, scalable, and future-ready architectures

Tech that speaks your language. Code that knows your compliance.

That’s the Liorta way.

Be ready, stay ready — with Liorta by your side.

Inspections aren’t just events – they’re stress tests for your systems, teams, and processes. At Liorta, we provide end-to-end inspection readiness and audit support services tailored for global regulatory landscapes including FDA, EMA, PMDA, MHRA, and ICH.

From pre-inspection prep to post-audit CAPA execution, we work alongside your QA, IT, and PV teams to ensure alignment, evidence readiness, and process transparency. We simulate inspection scenarios, conduct documentation reviews, and support system audits – internal, vendor, and client-side.

During live inspections, our domain experts provide real-time facilitation and response management, ensuring you’re always one step ahead. Post-inspection, we support RCA documentation, CAPA development, SOP realignment, and complete audit trail reviews.

• Pre-inspection readiness (GVP, GMP, J-GVP, GPSP, etc.)
• Live inspection management for critical/for-cause audits
• Third-party, system, and process audits
• Internal audits & gap identification
• RCA/CAPA strategy & SOP refinement
• PMDA, MHLW, EMA, MHRA inspection prep & response

With Liorta, inspections aren’t feared — they’re aced.

We help you move from compliant to confidence-ready.