InterPro QRA is a dynamic, global consulting practice specializing in CGMP compliance and FDA regulatory adherence. We deliver comprehensive solutions to pharmaceutical/biologic companies of every size. Our team is uniquely qualified to help clients steer clear of compliance and regulatory problems, and to quickly correct any that may arise. We have a collective 30-year history of working for the FDA - as boots-on-the-ground senior staff, directly involved ion issuing and resolving FDA enforcement actions. We bring the insight-and foresight-that only comes from having been on the other side of the table. Having actively conducted FDA inspections worldwide, we understand the nuances of regulations and how they're interpreted. We're quick to spot red flags. Significantly, our FDA experience is recent, so we can provide advise based on the most current FDA expectations of the pharmaceutical industry.