Regulatory Affairs
Today’s Regulatory Affairs Leaders are loaded with tasks to perform during a week. These tasks can include meetings, calls, coaching, submissions, preparation of responses, team management, and let’s not forget the hundreds of emails. Many companies today no longer can produce a product for just one country but need to support over 150 countries. Regulatory Affairs Leaders must ensure their innovative therapies and devices can be sold in multiple countries’ marketplaces. This is where IntePros can help. IntePros’ Regulatory Affairs Practice has been Nationally recognized for its work in the Medical Device, Pharmaceutical, and Biotechnology regulatory verticals. We specialize in Project-based Solutions and Consulting engagements and have a team of Regulatory Affairs Subject Matter Experts ready to support you.
