of a promising new drug or medical device, to the actual delivery of product to the market, virtually every step in the process involves compliance with federal regulations - the FDA, a fact of life that makes time a relentless adversary. EHKrohl Consulting, Inc. helps companies reduce the time it takes to put their products on the market by educating and assisting Quality Assurance personnel in implementing Compliant Quality Systems.
We specialize in assisting pharmaceutical, biotechnology, biologics, medical device, and their affiliated industries with Good Clinical, Good Laboratory, and Good Manufacturing Practices compliance (GxP).
EHKrohl Consulting, Inc. works closely with a client's quality assurance and management staff , forming a strategic partnership, dedicated to the goal of FDA quality compliant systems.
Once the EHK / client partnership is in place, a reduction in cycle time for the FDA approval process can be achieved, leading to a competitive advantage in the marketplace.