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.
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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
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Trial Design and Development
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Site Identification, Qualification, and Feasibility
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IRB/IBC Oversight
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Budget/Contract Development and Negotiations
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Site and Patient Training and Engagement
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Consulting
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
E-Book
Single IRB Review: Tips for Sponsors and CROs Working with Institutional Sites
This eBook provides a toolkit to understand the institutional review board's role when sIRB review is utilized.
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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.
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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
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3 min. read
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