Lecuyer Consulting

In the ever evolving landscape of pharmaceutical research and development, it can be difficult to know where to start with the most important step, ensuring patient safety.

This is even more difficult due to the nature of the regulatory agency guidance. Vague statements in the International Conference on Harmonization (ICH) guidelines provided by the FDA can cause confusion and reason for concern for even the most experienced company leaders. Lecuyer Consulting is here to help with all of your clinical trial safety data oversight needs.

List - ICH guidance documentsguidance, good clinical practice, ICH, trials, research, investigator, sponsor, monitor, IRB, institutional review board

With real world experience, we can help tailor processes and tools to your specific needs. Putting patient safety first is our top priority, which will ensure your ability to get your effective treatments to market faster.