Data integrity is an ever-increasing concern in the life sciences as evidenced by the recent activities of the FDA placing its watchful eye on the evolving medical device industry.
To help manufacturers better understand, establish, and maintain data integrity under growing regulatory scrutiny, Lachman Consultant Services, Inc. (Lachman Consultants) hosted a free webinar on Wednesday, December 1st, entitled “DATA INTEGRITY: Manufacturing & Quality,” presented by Mr. Scott Deckebach, Director in the Compliance practice at Lachman Consultants, and a life sciences and medical device regulatory compliance manufacturing, and technology expert, with more than 25 years of experience in the industry.
The webinar explored a range of important topics that included today’s most critical data integrity concerns, a four-step program for data integrity improvement, and the risk of not knowing the risks related to data integrity.
As Mr. Deckebach explained to those who attended, “Navigating the maze of rigors, safeguards, and protocols needed to maintain integrity and quality requires a comprehensive approach that includes robust processes and a dedicated adherence to their continuous application.”
If you were not able to attend or would like to listen to it again, you can access a replay of the webinar here.
