Content Packages Accelerate MBR Creation - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Content Packages Accelerate MBR Creation


Pharmaceutical Technology
Volume 38, Issue 2, pp. 12
Werum Software & Systems has expanded its PAS-X content packages with PAS-X MBR Design Elements content packages. The PAS-X MBR Design Elements Content Packages accelerate the creation of master batch records (MBRs) and help to assure higher quality MBR design in the configured system. The MBR Design Elements are templates for the creation of MBRs for specific processes in pharmaceutical and biopharmaceutical production such as granulation, IPC testing, or reconciliation. The Design Elements focus on the most efficient use of PAS-X functionality MBR, and are designed to operate with with PAS-X manufacturing execution system software. They are part of specific libraries available for all major manufacturing types, such as solids, liquids, and packaging. In addition, Uiversal Elements cover general processes that are not related to specific manufacturing types. The content packages provide a framework for standardizing processes within or between different plants.

Werum Software & Systems AG

ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
What role should the US government play in the current Ebola outbreak?
Finance development of drugs to treat/prevent disease.
Oversee medical treatment of patients in the US.
Provide treatment for patients globally.
All of the above.
No government involvement in patient treatment or drug development.
Finance development of drugs to treat/prevent disease.
24%
Oversee medical treatment of patients in the US.
12%
Provide treatment for patients globally.
10%
All of the above.
44%
No government involvement in patient treatment or drug development.
10%
Jim Miller Outsourcing Outlook Jim MillerCMO Industry Thins Out
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerFluorination Remains Key Challenge in API Synthesis
Marilyn E. Morris Guest EditorialMarilyn E. MorrisBolstering Graduate Education and Research Programs
Jill Wechsler Regulatory Watch Jill Wechsler Biopharma Manufacturers Respond to Ebola Crisis
Sean Milmo European Regulatory WatchSean MilmoHarmonizing Marketing Approval of Generic Drugs in Europe
FDA Reorganization to Promote Drug Quality
FDA Readies Quality Metrics Measures
New FDA Team to Spur Modern Drug Manufacturing
From Generics to Supergenerics
CMOs and the Track-and-Trace Race: Are You Engaged Yet?
Source: Pharmaceutical Technology,
Click here