Having the right team makes all the difference

Suzanne H. Heyd, MA, MFA

Suzanne is a professional medical writer and editor with more than 15 years of experience in medical communications. For the last 8 years, she has honed her expertise exclusively in the world of clinical trials disclosure, specializing in

• Protocol registration and trial results disclosure on public clinical trials databases such as ClinicalTrials.gov and (most recently) EudraCT
• Writing and updating SOPs and other formal documents related to transparency and disclosure activities
• Compliance audits of company-wide disclosure programs
• Advisory roles on the evolving disclosure requirements in US and EU
• Training of in-house and outsourcing staff on disclosure activities

An active member of the Drug Information Association’s Clinical Trial Disclosure community, Suzanne has chaired a subgroup on disclosure of observational studies, led tutorials at national conferences, and participated on panels at professional association meetings.

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Suzanne’s Associates

Should you require a dream team of expert consultants dedicated to your disclosure project, Suzanne maintains close working relationships with a network of highly-respected disclosure and transparency experts with whom she collaborates when a large or multifaceted transparency project is requested.