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…
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.
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…
Human Research Protection Program Services
Advarra knows that one size does not fit all. Each research program is different, with unique needs and distinct personalities. We take time to carefully understand your process and then…
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…
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.
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…
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.
GxP Auditing, Compliance, & Specialized Consulting
Advarra's experts can work directly with your team to provide consulting and evaluation services related to Good Practices, quality assurance, regulatory compliance, and human research protection for research.
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:…