Lisa Tinsley, new Director at Lachman Consultant Services, Inc.

We are pleased to announce that Lisa Tinsley has accepted the position of Director in the Compliance Practice at Lachman Consultants, effective December 1, 2017.

Ms. Tinsley is a 25-year pharmaceutical compliance and remediation professional who has led global compliance and auditing teams, developed Quality leadership and strategies, and enhanced Quality Systems. She is well experienced with FDA inspection requirements, has expertise in site inspection readiness for various technologies including oral solid dosage forms, sterile products, and medical devices. While at Novartis she gained extensive experience with preparation of FDA responses as well as global remediation programs.

Prior to joining Lachman Consultants, Ms. Tinsley served briefly as Vice President Quality – Specialty doses at Catalent. A large part of her career was spent at Novartis where she held positions of increasing responsibility starting as Site Quality Head at the Duluth, Georgia location and culminating as Director Global Compliance and Auditing. Prior to Novartis she served as Site Quality Head and Laboratory Service Manager at Bausch & Lomb, as well as Drug Products Manager at Greer Laboratories. Ms. Tinsley began her career as an Analytical Chemist at Baxter Healthcare where she was promoted to QC Analytical Laboratory Supervisor.

Ms. Tinsley earned her B.S. in Zoology (Pre-Med) from North Carolina State University and is working towards her Masters Science Jurisprudence, Pharmaceutical and Medical Device Compliance, from Seton Hall School of Law.

We welcome Lisa to Lachman Consultants and wish her a long and successful career with our firm.

For nearly four decades, Lachman Consultants has been the leader in providing cost-effective consultation and remediation services to the worldwide pharmaceutical, biotechnology, biologic, medical device, diagnostic and dietary supplement industries. With its strong and extensive cadre of consultant specialists and an unparalleled management team, its Compliance, Science & Technology, and Regulatory Practices provide the most expert counsel and array of services available. Lachman Consultants is proud of its tradition of supporting industry efforts to develop and ensure safe, effective and high-quality medical products. It remains committed to helping the industry anticipate and address its challenges through the development and implementation of practical, sustainable and cost-effective solutions based on the integration of scientific principles, evolving regulatory expectations, and technology.

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