Frequently Asked Questions

Yes. We frequently collaborate with advertising agencies, PR firms, and creative partners to provide Regulatory review for creative concepts and copy. This ensures compliance before materials are submitted to brand teams or internal committees.

We also work with ad agencies who are using Generative AI to create content to ensure that brand and compliance guidelines are being met.

Absolutely. We offer customized training covering:

• FDA advertising and promotion requirements

• OPDP enforcement case studies

• Best practices for clinical trial recruitment

• Emerging trends in digital and social media promotion Our goal is to empower your teams to create compliant content from the start.

Most work will be done virtually. In some instances onsite may be warranted (e.g., scientific congress, training/coaching sessions) and we are perfectly willing to travel as needed. Travel expenses will be tracked and submitted for reimbursement according to client policy.

Each project will be scoped out according to the client's specific needs. The scope will include a project overview, estimated hours, length of project and estimated cost based on either billable hours or a flat rate fee. Training/Coaching sessions are typically billed at a flat rate and ongoing consulting will typically include a small retainer as part of the billable hours.

Connect with us today to start the conversation moving forward.