Meet our amazing team
Our team is extremely qualified to get your product, drug, or biologic to the finish line
SNOW CONSULTING brings 32 years of Regulatory and Pharmaceutical experience to bear in strategic solutions for the consumer. With work in all areas of the drug development process from the IND on through Post-Marketing, SNOW CONSULTING can guide you toward successful development of your product, through a robust Regulatory Strategy. This includes exploring expedited approval pathways, coordinating Health Authority interactions, review of documents, labeling strategy, Regulatory Risk Management, and helping to set-up a Regulatory Department where needed, including creating SOPs and procedures.
Susan (O’Brien) Snow BSc, MBA
Regulatory Affairs Expert- 32+ Years
Susan is a highly experienced regulatory sciences professional with over 32 years of global biopharmaceutical experience across multiple regulatory disciplines, therapeutic areas and regions, with expertise in biologics, CMC, oncology, immunology, hematology clinical development strategy. Susan has developed a proven track record of leadership, strategic thinking, agility, accountability, and consistent delivery of results. She is an experienced senior consultant supporting the Regulatory teams in both small start-up and larger biopharma environments.
Tim Snow
VP Business Development & Client Services
I am an “Out-of-the-box” thinker & conflict resolution specialist in business negotiation, contract negotiation. I am a Driver of Execution and proven business developer with a track record of growing business relationships through leadership of cross functional teams, outside vendors, & agencies, all with a bias for action.
Real-life results
