Outsource Pharmacovigilance to PharmaRelations

Outsource Pharmacovigilance to PharmaRelations: Compliance, Expertise and Technology
in One Scalable Solution

For small and midsize biotech companies, pharmacovigilance can quickly become a complex operational and organizational challenge that takes away attention from their key focus: to get a product to the market efficiently and responsibly. As clinical activities expand, safety data volumes increase and regulatory expectations grow. At this point, companies need a PV setup that is compliant, scalable and inspection-ready – without necessarily building a large in-house function. PharmaRelations helps biotech companies establish, run and scale their PV operations through a flexible outsourcing model that combines experienced PV professionals with a validated safety database and AI-enabled functionality designed to enhance efficiency and scalability in pharmacovigilance activities.

Why Outsource Pharmacovigilance?
Outsourcing PV gives small and midsize biotech companies access to specialist expertise, scalable resources, validated technology and proven processes — without the cost and complexity of building everything internally. Whether you need support for a specific project, QPPV services, case management, signal detection or a fully outsourced PV operation, PharmaRelations can tailor the solution to your stage, risk profile and ensure regulatory requirements.

More Than Consultancy: A Complete PV Solution
At PharmaRelations, we offer more than individual resources. We provide a end-to-end pharmacovigilance operating model that can include:

• Pharmacovigilance consultancy services
• Global and local PV support
• QPPV and Deputy QPPV services
• Case management and adverse event reporting
• Signal management and aggregate reporting
• Audit and inspection readiness
• Quality management support and regulatory guidance
• Validated and AI-enabled safety database
  

Advanced Safety Database and PV Platform
A key part of our outsourcing offering is access to a validated safety database designed for GxP-regulated environments. The platform supports end-to-end case management, reporting, and signal detection while ensuring compliance, traceability, and data integrity.

The system also includes automation and AI-capabilities for activities such as coding, narrative generation, and data processing, helping to reduce manual workload, improve quality, and increase efficiency. As the number of cases grows, its AI-enablement will save manual work and ensure further scale in your setup.

 A Trusted Nordic Partner
As a Nordic life science partner, PharmaRelations combines local market understanding,
deep PV expertise and modern technology.

Looking to set up or strengthen your PV operations?

Contact PharmaRelations to learn how our experts and validated safety database can
support your pharmacovigilance needs.

Nilla Juhlin, Nordic Head of PV
+46 70 165 22 28  nilla.juhlin@pharmarelations.se