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Research compliance is
an ongoing commitment.

Research Compliance

Enhance Your Site Operations and Research Compliance

Compliance with research is a continuous effort. It is the basis for moral research procedures. Our team of professionals assists you in navigating the many rules and directives issued by regulatory agencies within a dynamic and intricate regulatory environment.

Compliance with Research and Site Management

In accordance with federal regulations, state and local legislation, and industry best practices, our team will assist you in creating, putting into operation, and maintaining research compliance and administrative procedures.
Our team of experts collaborates with you to address the following issues:
  • Complex regulatory landscapes: We assist in negotiating the many rules and regulations from multiple institutions and governing bodies. Our team includes extensive expertise from R1 institutions.
  • Resource limitations: We collaborate with research administrations to offer temporary, skilled staff so you can scale operations as necessary to meet vital compliance standards.
  • Monitoring: To guarantee adherence to legal standards and data safety monitoring strategies, our team offers post-approval monitoring and auditing services.

Our Proficiency in Research Compliance

Sachin has been involved with research compliance for more than 7 years. He has overseen compliance for IEC, conflict of interest, HIPAA privacy, research misconduct, institutional biosafety, radiation safety, export control, and facility security programs at university medical centers, DCGI sponsored sites, and other organizations.

Our Research Compliance Expertise

Mr/ Mrs

SVP Consulting

Cheryl has over 20 years of experience in research compliance. She has provided compliance oversight to programs at academic medical centers, NIH funded sites and institutions including pre-clinical, IRB, conflict of interest, HIPAA Privacy, research misconduct, institutional biosafety, radiation safety, export control, and facility security. Prior to joining Advarra, Cheryl has served in senior leadership roles for Protocol Review, Monitoring Systems & Regulatory Affairs at a NCI-designated cancer center as well as in research compliance at a major research university.

Joshua Fedewa, MS, CIP
Director, Research Compliance

Faith Bertrand, CIP
Senior Consultant

Lisa Rooney, JD
Managing Expert

John Baumann, PhD, MA, BA
Managing Expert

Cynthia Hahn
Managing Expert

Jonathan Hunter, MA, CIP
Managing Expert