Compliant master manufacturing and batch production records are fundamental to your cGMP implementation, and they are probably the most important documents that FDA will examine to assess your firm’s quality system. If you don’t include all the elements required by 21 CFR Part 111 in your production records, you are at risk of receiving a Form 483 during your next inspection, or even a Warning Letter. This webinar will discuss the most common problems actually found in dietary supplement master manufacturing records by inspectors, and how you can fix them.