At Liorta, we specialize in delivering world-class IT and business consulting services tailored specifically for the life sciences industry. Our team of seasoned experts brings deep industry knowledge and technical expertise to help organizations navigate the complexities of Drug Safety, Regulatory Affairs, Medical Affairs, and more. Whether you are optimizing your operational processes, ensuring compliance, or enhancing your drug development lifecycle, we empower you to drive growth, innovation, and success with confidence.
With decades of collective experience in life sciences, Liorta offers unparalleled insight into the challenges and opportunities within the pharmaceutical and lifesciences sectors. Our consultants are not just technical experts; they are trusted advisors who understand the nuances of the industry from a strategic, operational, and regulatory perspective.
From Drug Safety to Regulatory Affairs and Medical Affairs, Liorta provides a full suite of consulting services designed to meet the unique needs of life sciences companies. We offer end-to-end solutions that help you streamline processes, improve efficiency, and maintain compliance in an increasingly complex environment.
We understand that no two organizations are the same. That’s why we take a personalized approach to every project, working closely with you to design bespoke strategies that align with your specific goals. Whether it’s improving pharmacovigilance systems or navigating the intricacies of regulatory submissions, our consultants are with you every step of the way.
In today’s fast-evolving life sciences landscape, the integration of technology is critical to staying ahead. Our IT consultants specialize in delivering innovative technology solutions that optimize data management, ensure regulatory compliance, and enhance operational efficiency. From electronic submissions to data analytics, we leverage the latest tools to provide you with actionable insights.
Strong track record of successfully partnering with life sciences organizations to achieve measurable outcomes. Our deep understanding of the regulatory landscape and our ability to execute complex projects means that we consistently help our clients reduce time-to-market, minimize risks, and drive operational excellence.
We believe in the power of collaboration. At Liorta, we work as an extension of your team, fostering open communication and close collaboration to ensure that solutions are seamlessly integrated into your operations. Our consultants are committed to working with you to achieve sustainable, long-term success.
Navigating the regulatory environment in life sciences can be challenging, but with Liorta, you can trust that compliance is at the forefront of everything we do. We stay updated on the latest industry regulations and standards, ensuring that your operations not only meet but exceed the required benchmarks for safety, quality, and compliance.
At Liorta, we focus on providing complete solutions for Argus Safety. Our services cover everything from smooth system implementations and precise upgrades to hassle-free migrations, ensuring that your pharmacovigilance system stays strong, efficient, and compliant with global regulations.
Implementing or upgrading a Safety Suite typically requires a significant cost and effort. However, our proven approach, refined over multiple implementations, enhances efficiency in all areas. This methodology is flexible enough to accommodate the unique needs of clients across different industries, from small businesses to large enterprises, while ensuring flawless execution. With our expertise in pharmacovigilance and a library of standard artifacts & solutions, we help reduce both costs and time.
At Liorta, we specialize in providing expert pharmacovigilance (PV) system migration services, ensuring seamless transitions across a wide range of industry-leading platforms, including Argus, ARISg, Perceive, IVP, CW5, and E2B systems. Our deep understanding of the complexities involved in PV system migrations allows us to deliver tailored solutions that minimize disruption, reduce risk, and maximize efficiency.
Our team of experienced consultants has successfully managed numerous migrations for clients across various sizes, ensuring compliance with global regulatory requirements while optimizing system functionality. We work closely with our clients to fully understand their unique needs, helping to define a clear migration strategy that aligns with business goals and operational requirements. Whether you’re upgrading to a more advanced platform, consolidating systems, or transitioning to a new system altogether, we have the expertise to handle the entire process—from planning and data mapping to testing, validation, and go-live support.
We prioritize accuracy, timeliness, and compliance in every migration, leveraging our vast experience to ensure that data integrity is maintained throughout the process. Our comprehensive approach minimizes operational disruptions and ensures that your PV systems remain fully compliant with industry standards, including E2B requirements and regulatory guidelines.
Partner with Liorta for a hassle-free, efficient PV system migration that drives performance, reduces risk, and supports regulatory compliance across your entire pharmacovigilance ecosystem.
Your Trusted Partner in Pharmacovigilance (PV) Reporting
At Liorta, we bring extensive experience in designing custom data warehouses and developing ETL connectors to seamlessly aggregate multiple data sources. Our expertise in Reporting and Analytics offers comprehensive solutions tailored to meet both global and Japan-specific regulatory requirements.
Our team of seasoned professionals has successfully developed and implemented both Commercial Off-The-Shelf (COTS) and custom reporting solutions. We go beyond initial report development, providing ongoing support with ad-hoc and aggregate reporting services to ensure compliance, efficiency, and insightful decision-making.
At Liorta, we follow a highly efficient and streamlined report development process, ensuring accurate, timely, and insightful reporting that meets evolving industry regulations. Whether you need periodic safety reports, compliance-focused analytics, or custom dashboards, our expertise positions us as a trusted partner for all your PV reporting needs.
Let Liorta empower your organization with intelligent, regulatory-compliant reporting solutions.
