Clinical Research
It’s time you partner with an attorney who understands you.
Sponsors and CROs have lawyers.
Why shouldn’t you?
Clinical Research Sites are a critical part of the research ecosystem.
Our clients benefit from our firsthand knowledge working in clinical research administration.
We know where your blindspots are and protect you from the “known” unknowns.
From subject recruitment to Clinical Trial Agreement (CTA) and study budget negotiations, count on our expertise to guide you to success.
Research Compliance is not something to worry about after the Food & Drug Administration (FDA) shows up at your site.
Work with us to ensure you are compliant and confidently prepared for any inspection or audit.
Below are some examples of the ways
we can help you:
Clinical Trial Agreements (CTAs)
Clinical Research Compliance
Principal Investigator (PI) Services Agreements
Study Budget Negotiations
Study Subject Recruitment Plans
Research Privacy (HIPAA, GDPR, and Beyond)
Artificial Intelligence (AI) and Data Rights
Data Commercialization
Confidentiality Agreements (CDAs)
Non-Disclosure Agreements (NDAs)
And all other contracts and compliance matters involving
clinical research and grants.
Ready to work with an attorney who understands you?
Contact us.