For data integrity requirements, which are urgently needed in the pharmaceutical industries, it is necessary to ensure that there are no data loss or inconsistencies throughout the data life cycle, from the generation of electronic data to its disposal. In addition, there is 21 CFR Part 11 established by the FDA as a regulation for electronic records and electronic signatures, which requires prevention of falsification of electronic records and retention of change records.

Anritsu’s Checkweigher can meet the requirements of 21 CFR Part 11 by incorporating various functions such as user authentication, audit trail, and data encryption / decryption. In addition, since it is equipped with a large 15-inch touch panel, you can check production data and statistical records on a large screen. With abundant guidance functions, even beginners can operate the Checkweigher easily and confidently. Please watch the following video to see how the above features work with the actual machine (Video: Produced in March 2021).