Discrepant Material Report (DMR) for Life Sciences

Make sure your discrepant material report is accurate and timely.

Good manufacturing practice (GMP) rules require complete and accurate documentation. The discrepant material report (DMR) records all occurrences of nonconforming materials. The report is a crucial document for manufacturers. MasterControl Manufacturing Excellence can help manage DMRs and related documentation. Quickly identify, investigate, and resolve discrepant materials.

Free Resources
Effective Nonconformance Management Key to FDA and ISO Compliance
Download