We are pleased to announce that Michelle Ryder has accepted the position of Principal Consultant in the Regulatory Practice at Lachman Consultants, effective October 28, 2019.
Ms. Ryder is a seasoned Regulatory professional with more than 20 years of experience in the pharmaceutical industry. She has provided strategic leadership and plans for ANDA, NDA, and IND applications for various dosage forms and formulations, and has led the entire project lifecycle from product feasibility assessments through post-approval changes and compliance.
Ms. Ryder joins us after ten years of employment at Tolmar Inc. where she served in roles of increasing responsibility culminating as Vice President, Regulatory Affairs. Prior to joining Tolmar, she did some regulatory consulting, was a Regulatory Associate at Geneva Pharmaceuticals, and a Research Associate / Regulatory Associate at Synergen, Inc.
Ms. Ryder earned her B.S. Microbiology from Colorado State University.
