CFR21 compliance of the STARe Software - METTLER TOLEDO

On Demand Webinar

CFR21 compliance of the STARe Software

The CFR STARe software option allows the user to work with a compliant system under FDA regulations. The purpose of FDA regulations is to ensure the integrity, trustworthiness and reliability of electronic records.

METTLER TOLEDO's STARe software complies with the challenges presented by the FDA regulations, such as managing the record, data backup, audit trails, security and access control.

In this Webinar, we will introduce the requirements assigned by FDA related to electronic data management system and our METTLER TOLEDO solutions to keep your thermal analysis work with ease and satisfactorily in regulatory environment.

English

21 CFR Part 11 is set of regulations which provides criteria for acceptance of electronic records and electronic signatures as equivalent to paper records and handwritten signatures executed on paper.

In this web-based Seminar (Webinar), we will present the features of CFR STARe software and how METTLER TOLEDO approaches to the assessment and compliance to the challenges for 21 CFR part 11 regulations.

The Webinar covers the following topics:

  • Introduction
  • What is 21 CFR part 11?
  • Requirements for compliance
  • Features of STARe software
  • Features/ Solutions of Stare software
    - Access control
    - User Level management
    - Electronic records
    - Audit Trails
    - System Validation
    - Connectivity to LIMS
  • Summary
 
 
 
 
 
 
 
Thank you for visiting www.mt.com. We have tried to optimize your experience while on the site, but we noticed that you are using an older version of a web browser. We would like to let you know that some features on the site may not be available or may not work as nicely as they would on a newer browser version. If you would like to take full advantage of the site, please update your web browser to help improve your experience while browsing www.mt.com.