Pharmaconnect gets down to business. We help pharmaceutical companies get their regulatory documents submitted and up to compliance in a variety of different drug industries within the US and Globally.
Examples of the services we can provide: •IND (Investigational New Drug) Regulatory Document Construction, editing, and advising. •FDA or equivalent Meeting Preparation regarding New Drugs or Drug Product models. •General Regulatory Questions and Consulting
Document preparation is an integral part of the drug approval process and interactions with FDAs across the globe. Let us help with complicated regulatory environments.
We are a Northern-Chicagoland based consulting firm equipped with the tools and brains to help make your Regulatory CMC process a success.
Our team's background draws together decades of corporate Regulatory experience and expertise. Our team descends from the Executive Director level of Regulatory Affairs.
Pharmconnect connects you to the best talent to bring the best solutions for your Regulatory client or team.
We know your drug product can make a difference where it needs to.
That's why we can help get it available across the world.
With global Regulatory CMC experience on our consulting team, we can help with INDs, FDA Questions, and New Drug submissions in the U.S. and Globally.
Whether you're a recruiter or a corporate regulatory professional, get in touch with our team. Submit your information below and tell us a little bit more about your project!
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