x

Join Advarra

Learn more about our company team, careers, and values. Join Advarra’s Talented team to take on engaging work in a dynamic environment.

See Jobs

Enable Growth and New Product Development

Advarra’s biopharma and medical technology solutions are solely focused on helping emerging and mid-sized biotechnology, pharmaceutical, and medical technology and device companies achieve their development objectives.

Contact Us to Get Started

Site Building with gear to signify operations and easy 1 2 3 callout steps

Optimize your clinical development with Advarra’s services and solutions

  • Novel, sometimes complex, products utilizing innovative science or technologies
  • Compressed development timelines often driven by funding milestones
  • Additional expertise or resources needed to augment critical capabilities
  • Limited capacity to manage multiple service provider partnerships

How Advarra Helps:

Efficient IRB review and approval

  • 20 IRB meetings per week to facilitate the rapid turnaround of expert review and approval documents
  • Relationships with over 3,500 institutions, hospitals, health systems, and academic medical centers

Biosafety compliance for genetically engineered treatments and vaccine research

  • The largest comprehensive network of pre-registered and vetted Gene Therapy Ready sites

Access to additional expertise and staff to fill gaps, as necessary

  • Network of 6,500+ industry experts and professionals with hands-on life sciences experience in clinical, regulatory, and quality

Service provider relationships based on trust, transparency and ease of use

• Single point of contact and dedicated customer experience team to manage all your needs

Featured Resources

 
Webinar

Thorny Issues in Medical Device Research

Learrn how to navigate thorny issues in medical device research, including which regulatory requirements apply to different types of device studies.

Watch Now
Read more
 
Blog

Study Startup Success for BioPharma and MedTech: Engage a Research Compliance Partner

Engaging with an expert research compliance partner throughout the clinical development process allows researchers to focus on what matters

Read Now
3 min. read
Read more
 
E-Book

Central IRB Review for Institutional Sites: A Toolkit for Sponsors and CROs

January 22, 2021

Read Now
Read more

Visit the Resource Library

Ready to make your research safer, smarter, faster?

Contact Us