Info Sheet

Research Billing Compliance

Advarra Consulting’s research billing compliance services use industry standard methods combined with national and regional coverage determinations and proprietary solutions to ensure your organization stays in compliance with Medicare billing ...

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Calendars Info Sheet

Learn why 100% of our customers would recommend Advarra Protocol Calendars to other organizations in the industry.

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Info Sheet

Payments Info Sheet

Advarra Participant Payments is an automated system that helps organizations, CROs and sponsors immediately pay subjects after each visit.

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Info Sheet

Phase I Services

Advarra offers the most comprehensive approach to Phase I research with experience overseeing thousands of Phase I studies in the US and Canada.

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Data Protection & Compliance Services

With the growing prevalence of technology in research, compliance with Part 11 is increasingly critical, but many organizations aren’t aware that they’re required to be Part 11-compliant. Ensure your organization ...

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Info Sheet

Research Administration

Strong research administration infrastructure is critical for success in today’s ever-growing and consolidating research industry. Advarra helps you move your research forward by recognizing and confronting the challenges of drug ...

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Protocol Development & Medical Writing

The Advarra team provides medical, scientific, and regulatory expertise in human subject research. We pride ourselves on our proven methodology, quality of work, and customer service.

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Regulatory Consulting

Advarra's regulatory consultants take action and move your research forward. If you’re looking for help in the development of innovative life science and digital health products, then Advarra is the ...

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Info Sheet

Clinical QA Consulting For Medical Device Research

The medical device experts at Advarra can help you navigate the regulatory environment to ensure compliant, high-quality clinical study conduct.

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Electronic Study Design Services Overview

Advarra’s team of study design experts deliver high-quality calendars and forms in Advarra EDC utilizing best practices in data capture and form design.

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Info Sheet

Revised Common Rule Quick Reference

Most requirements for the revised Common Rule, the federal policy for the protection of human subjects in research, went into effect on January 21, 2019. This reference will help you: ...

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Info Sheet

CQA Compliance Oversight Programs

Advarra's customized evaluation and support services for clinical quality assurance (CQA) compliance help ensure your organization maintains appropriate compliance with applicable regulations and good clinical practice (GCP).

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