Excelya Wrap 2025. A snapshot of our growth innovation and impact View inside
Submit your request

Partner with Excellence

Global PV & Safety

Control · Transparency · Flexibility · Dedication

Expert pharmacovigilance and safety services with 20 + years experience, strong quality record, and tailored support from detection to risk management across drugs, devices and cosmetics.

16

Global footprint

Offices across the US, Europe, and Asia with 25 plus countries covered.

1000+

Specialists

Global teams with strong European roots supporting your trials.

Key areas of expertise

Domains where Excelya delivers consistent, high quality outcomes.

Clinical operations PV and safety Data management Biostatistics programming Medical affairs Regulatory affairs Quality assurance eTMF management

Our certifications

Ecovadis certification
ESYD certification

Why Excelya?

90+ DEDICATED PV & SAFETY EXPERTS

Highly trained professionals supporting global pharmacovigilance companies with strong expertise in patient safety and compliance, including clinical safety management.

EXTENSIVE FIELD KNOWLEDGE

Managed and completed over 300 projects delivering pharmacovigilance services Europe-wide, supporting sponsors across multiple therapeutic areas with strong expertise in risk management in pharmacovigilance.

QUALIFIED TEAM MEMBERS

Highly qualified team (Master, PhD) with 20+ years’ experience in safety monitoring services across clinical and post-marketing environments and providing drug safety outsourcing support when needed.

KNOWLEDGEABLE STAFF

Excelya assigns experienced pharmacovigilance experts Europe based, ensuring consistent quality and local regulatory understanding.

Strengthen your pharmacovigilance

Our PV capabilities

Biotech and Midsize

Your dedicated safety partner from first-in-human through Phase III and beyond approval, delivering best-in-class pharmacovigilance services and supporting pharmacovigilance in biotech.

  • One expert provider to manage your safety data

  • Specialist biotech solutions to meet your needs

  • Knowledge of early phase and post-approval challenges and unique safety requirements

Pharma Development

Your functional service provider safety partner for clinical development and marketed products, with expert pharmacovigilance consulting and tailored drug safety solutions when specialized approaches are required.

  • Flexibility and scale, onshore, nearshore and offshore , including expert global hubs

  • Cost-efficient safety management

  • Trusted pharmacovigilance providers supporting clinical and post approval programs.
  • Expert knowledge of your challenges and how to address them

Marketed products

Your local PV team, available for your marketed products in 50+ countries, offering international support including pharmacovigilance reporting services and drug safety monitoring.

  • International coverage, with people on the ground in each country
  • Experts who understand the local requirements and context
  • Cost-effective pharmacovigilance solutions that uphold the highest compliance standards for mid to small pharma.
Do you have any questions?

Frequently Asked Questions

Are you an SME looking for a vigilance partner?

At Excelya, we deliver comprehensive pharmacovigilance solutions tailored to your scale through both Full Service and FSP delivery models.

Do you need local vigilance support?

Excelya supports pharmacovigilance activities in more than 25 countries, including local regulatory requirements and Qualified Responsible Persons for Pharmacovigilance.

Are you looking for a reliable vigilance partner for your development program?

Excelya supports the full vigilance lifecycle, from ICSRs and aggregate reports to safety protocol and IB CSR contributions for robust risk assessment.

Do you need reliable and efficient project management for vigilance activities?

Excelya’s experienced project managers take ownership of your vigilance projects from setup or mid phase and guide them through successful completion.

Is your biotech company seeking vigilance support from Phase I to market registration?

Excelya supports the full vigilance lifecycle, from ICSRs and aggregate reports to safety protocol and IB CSR contributions for robust risk assessment.

Are you looking for reliable and efficient project management?

Minimize issues and effort. Our experienced project managers will take control of your project from set up or from where you need and will lead it to a successful completion.

How can you retain and strengthen pharmacovigilance knowledge within your organization?

Excelya offers webinars, white papers, and tailored training programs designed to strengthen internal expertise and long term compliance.

How can you retain and strengthen pharmacovigilance knowledge within your organization?

Excelya offers webinars, white papers, and tailored training programs designed to strengthen internal expertise and long term compliance.

Excelya applies 20 years of Pharmacovigilance experience

Submit your request