Prior to starting PharmAffairs Consulting, Linda served as Director of Regulatory Affairs for Regulatory Compliance Associates, and as Senior Regulatory Affairs with Hospira, Inc. She has 30 years of pharmaceutical industry experience and pharmaceutical associates to rely on.
As a Regulatory Affairs Consultant, her responsibilities include evaluating and preparing global regulatory strategies and providing the required inputs for marketed drug products and generic drug programs. She serves as a Regulatory Affairs subject matter expert and provides input for successful development, filing, approval, implementation, and remediation work associated with projects. Additionally, her strengths include project management, corrective action, new technology, quality assurance, and streamlined manufacturing and processing initiatives.
Contact Information:
Linda Biava
Vernon Hills, IL 60061
847-732-9412
info@PharmAffairs.net