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New Webinar Series From Lachman Consultants Provides Valuable Information To The Pharmaceutical Industry

Ever a responsive and supportive partner to its clients, these webinars are Lachman Consultants latest effort in providing timely and critical information to life science organizations as they navigate the ever-changing economic and business environment, further complicated by social distancing and health safety concerns.

“Providing the most up-to-date actionable guidance and information has been a keystone of our long-standing client relationships,” commented Ricki A. Chase, M.S. Executive Director in the Compliance Practice, Lachman Consultants, stated. “These webinars enable Lachman’s team of SMEs and industry experts to bring their unmatched knowledge and expertise to life science organizations at a time when they can benefit from them the most.”

The first two webinars in the series focus on FDA inspections. The initial installment, entitled “Preparing for and Handling an FDA Inspection,” will be hosted by Ricki Chase, former FDA Director of the Investigations Branch in the Chicago District. Ricki will be joined by Linda Evans O’Connor, Vice President, Chief of Staff, Lachman Consultants.

The hour-long “Preparing for and Handling an FDA Inspection” webinar will help organizations comprehensively plan for and navigate the various stages, details and technicalities before, during, and after an FDA inspection. Among the topics discussed will be an overview of the FDA and GMPs, FDA Inspections and Enforcement Actions, and the various steps in organizing for an FDA Inspection.

The second Lachman Consultants’ webinar in the series, “How to Respond to Inspectional Observations” will be held on Thursday, May 21st at 2:00 pm EDT and will also be hosted by Ricki Chase, former FDA Director of the Investigations Branch in the Chicago District. Joining her will be Linda Evans O’Connor, Vice President, Chief of Staff, Lachman Consultants. Topics for this webinar will include responding to 483s, summarizing a commitment to sustainable compliance, providing corrective actions, and establishing a practical timeline.

For more information about Lachman Consultants’ webinars, visit:

To sign up for “Preparing for and Handling an FDA Inspection,” please go to:

To sign up for “How to Respond to Inspectional Observations,” please go to:

2020 © Lachman Consultants


Founded in 1978, Lachman Consultants maintains three practice groups: Compliance, Regulatory Affairs, and Science and Technology. Each practice offers industry-leading experience and expertise in its area of focus. Lachman Consultants serves emerging-to-enterprise organizations on a worldwide basis in the Pharmaceutical, Biotechnology, Biologics, Device, and Related Life Science Industries. Lachman Consultants deliver highly effective and proven solutions that include FDA-Related Services, Audits, Quality Assurance & Controls, Scientific and Technical Assistance, Systems Evaluation, and Training, which have been shown to consistently exceed client requirements and expectations.

For additional press information, please contact:
Ilena Della Ventura
Delia Associates
T. 908-534-9044

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