Rebecca Welton

Senior Consultant, Regulatory Affairs, Lachman Consultant Services, Inc.

Rebecca (Becky) Welton is a Senior Consultant in the Regulatory Practice at Lachman Consultants who is an experienced Science, Operations, and Regulatory leader with 30+ years in the pharmaceutical industry. She has held positions of escalating accountabilities in chemistry, formulation development and management, pilot plant manufacturing, and regulatory affairs. She is well versed in areas of product development, leadership, regulatory strategy, and pre- / post- approval regulatory affairs support of Chemistry, Manufacturing, and Controls (CMC) for human and veterinary products including: solid dosage, liquid oral solutions, topical solutions, and sterile (small and large volume), terminally sterilized, aseptically processed, and lyophilized products. Becky led the authoring team for the ISPE Guide “503B Compounding – Regulatory Basis and Industry Good Practices for Outsourcing Facilities”