Let our experienced consultant at LVM Pharmaceuticals Consulting, LLC provide the consultation services your company requires. Trust that we’ll pay great attention to every detail of our research. We provide input on every phase of clinical drug development, the ramifications of preclinical findings, and other services. Read on to learn more about the other services our company provides.
Input (proactive and/or critical review) of clinical portions of FDA briefing documents including preIND, IND, preNDA packages
Input (proactive and/or critical review) of all clinical aspects of drug development pre-approval
Design and analysis of clinical trials
Input on clinical ramifications of preclinical findings
Input on requirements and preparation for interactions with the FDA
Support for Scientific Advisory Committee meetings
Post approval support including safety-related issues
Participation in Conferences/Workshops