At ECG, we have been helping drug and device development teams prepare for health authority interactions since the 1980s. We work with your team to identify objectives, create a persuasive communication strategy, and strengthen delivery. Our Principals have helped teams prepare for FDA, EMA, Health Canada, KIKO/PMDA, and the Chinese Ministry of Health – or in some cases, several of them at once.
When your team is preparing for the regulatory approval process, there may be several stops globally on your path to success. ECG can help ensure consistent key messages permeate written materials/submissions, the presentation, and Q&A Books to strengthen accuracy, consistency, and emphasis for all submissions, globally, throughout the process.
We offer a wide range of services for any critical healthcare meeting, virtual or face-to-face:
Please contact us via email or at +1-201-894-8200 to discuss the custom communication strategy we can create for your upcoming global regulatory submissions.
