Transform your PV Processes with our End-to-End Services and Cutting-Edge Technology

At Navitas Life Sciences, we harness the power of artificial intelligence and advanced processes to enhance drug development and deliver holistic solutions, tailored to your specific needs. As a full-service pharmacovigilance (PV) provider, we cover the entire PV Value chain, from case intake to safety risk management. Our global presence, with centers in the US, EU, and India, ensures a reliable mix of offshore and onshore teams to meet all of your PV needs.

Supported by our team of Qualified Persons Responsible for Pharmacovigilance (QPPV), Safety Medical Experts, and PV Subject Matter Experts, we provide unmatched expertise, guiding you through every stage of your PV processes to deliver on quality and compliance.

With 30+ years of proven PV consulting experience, we have partnered with the top 300 pharmaceutical companies to enhance processes, IT infrastructure, and sourcing strategies. This is further supported by our industry-leading PV networks, pvnet^®, pvconnect^®, pvtech^®, and pvindia^® through which we have delivered unparalleled PV insights and benchmarking for some 20+ years. This expertise ensures our services meet high standards for compliance, quality, and efficiency.

Our End-to-End PV Services include:

Full QPPV Services

Global Network, Local Experts

Signal Management as a Service (SMaaS)

Detection, Validation, Assessment, and Tracking

Medical Information Contact Center

Utilizing a global platform, we provide local expertise

Literature Monitoring as a Service (LMaaS)

Delivering Safety across the product life cycle

Risk Management as a Service (RMaaS)

Identifying, characterizing, preventing, and mitigating risks

Advanced Technology for Enhanced Efficiency

Our End-to-End PV services are fully automated and powered by cutting edge technology. Leveraging AI and Robotic Process Automation (RPA), our solutions are designed to streamline every aspect of the PV process. Partnered with industry leaders, and bolstered by our proprietary innovations, we address critical gaps in PV to deliver unmatched service and support. safetyREADY^® offers a fully compliant and validated suite of services to ensure seamless and efficient PV processes:

Intake and Triage of all case reporting sources
PV Database Integration utilizing industry-standard products from Oracle and other leading vendors
Quality Control to maintain the highest standards of compliance
Dashboard and Analytics for real-time insights and decision-making
Aggregate Report Development and Management for efficient reporting
Signal Management to identify and mitigate potential safety risks

In addition to our core PV services, we provide best-in-class tools and integrations, including:

Literature Monitoring powered by Biologit for comprehensive safety data review
Clinevo MICC Database for streamlined medical information management
Safety Report to Sites and Committees to facilitate transparent communication
Axway eSubmission Gateway for seamless regulatory submissions

With our advanced technology and expert-driven approach, Navitas Life Sciences empowers organizations to optimize their pharmacovigilance workflows, ensuring both safety and efficiency in regulatory compliance.

ARTICLE

Automation of literature search and review

Over the years, pharmacovigilance (PV) processes have relied on PV professionals manually sifting through large volumes of data to identify, assess, and report Adverse Event (AE) information.

ARTICLE

The crucial role of PV in combatting counterfeit drugs

It would be possible to put a stop to counterfeit medicines. However, simple controls are often still lacking. That's why researchers want to help drug detectives.