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Genedata Biologics 3.0 Boosts Efficiency Through Standardization
Date:1/21/2013

s candidates and their history,” said Dr. Othmar Pfannes, CEO of Genedata. “The standardization of these views and the underlying automated data processing minimizes duplication of work, eliminates error-prone manual activities, and provides extremely valuable transparency across an organization for efficient decision making. Our insight into standard processes and best practices has driven the development of Genedata Biologics, which is becoming the data management platform of choice for innovative biologics R&D organizations.”

Genedata Biologics V 3.0 is available now and shipping directly from Genedata.

Editorial Note: PepTalk 2013 -- “Antibodies for the 21st Century Track” -- Thursday, January 24, 2013; 10:45 am-11:15 am.

Genedata Biologics V 3.0 – Highlights

  • Data Management & Access Control Framework: New user group infrastructure provides a fine-granular mechanism to control access to sensitive data in a collaborative environment. The system now supports cross-departmental and external data exchange with CROs and CMOs, as well as technology transfers among research partners, which is of vital importance in IP-critical environments.
  • Flexible Reporting Engine: New framework for generating customized reports for scientists, project managers, technicians, and management. Easily generated reports can now be tagged for keywords and relationship (e.g. reporting all cell lines stably expressing Fab-Fvs), research stage and success of results (e.g. portfolio of leads across different screening efforts), or grouped with data, e.g. Protein Expression Batches along with expression levels, vector information (i.e. signal peptides, promoters), or antibody germline sequence information (i.e. IGHV1-24). Typical examples also include KPIs (e.g. real-time overview of the number of candidates successfully expressed and purified, with a monthly break-down), and dashboards for facilitating de
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