Lachman Consultant Services
Sharon Trombley is a Senior Associate in Regulatory at Lachman Consultant Services with vast experience in medical technology, regulatory affairs, clinical trials, and document specialist roles. During their time at MMS, Sharon held the position of Senior Regulatory Operations Specialist II. Prior to this, Sharon worked at QuatRx as an Operations Assistant focusing on document specialist tasks, and at Pfizer as a Senior Document Specialist managing various documents for drug submissions. Sharon has a strong background in publishing regulatory submissions and ensuring compliance with standards such as ICH eCTD format.
Lachman Consultant Services
Experience. Excellence. Founded in 1978, Lachman Consultants serves companies in Pharmaceutical, Medical Device/Combination Products, Biologics, and Regulatory Affairs. Each practice offers industry-leading experience and expertise in its area of focus. Lachman Consultants serves emerging-to-enterprise organizations on a worldwide basis, delivering solutions that include FDA-Related Services, Audits & Mock Inspections, Quality Assurance & Controls, Scientific and Technical Assistance, Systems Evaluation, Regulatory Affairs, and Training, which consistently exceed client requirements and expectations. When it comes to compliance and regulatory affairs, Lachman has set the industry standard through senior consultants, efficient engagements, integrated expertise, and loyal clients.