Life Sciences

Companies in the Life Sciences vertical are challenged with rigorous compliance requirements and intense industry competition. Vesta Partners has a rich background of helping companies meet those regulatory and business needs through the implementation of SAP EAM and adoption of our VTEAM maintenance best practices.

Vesta has expansive experience with customers in the pharmaceutical, biotechnology and medical device industries implementing best practices in the areas of work management, master data management, calibration and configuration management, among others. As such, we are intimately familiar with the additional rigors that accompany validated software solutions, such as supporting good clinical, laboratory and manufacturing guidelines (GxP), as well as regulations such as 21 CFR Part 11 for the management of electronic records (e.g. audit trails, electronic signatures).

Furthermore, Vesta understands the significant impact that validation has on the scope and timeline of an SAP EAM implementation project, including:

• Validation protocols
• Requirements tracking
• Custom development
• Data conversion
• Training
• Testing

Our focus on this industry is further illustrated by the investment and development of Vesta QMC – a calibration solution that reduces inherent complexities and offers additional flexible functionalities to create a seamless process for the maintenance organization.