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2nd Annual Pharmaceutical Manufacturing Execution Systems Conference

May 22-23, 2017 | San Antonio, TX

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ABOUT THE CONFERENCE

Exploring topics of pivotal importance such as the practical application of change management strategies for evolving MES projects, this conference provides a tremendous opportunity for industry to come together & discuss solutions to critical challenges. In addition, case study sessions will provide the audience with an enhanced understanding of strategies for change control processes for master batch records across interface applications. Throughout the program, presenters will share best practices, engaging with the audience to discuss the development of a robust MES plan where organizations can support the shared goal of producing safe & effective pharmaceutical products. Combining educational program content & optimal networking, the Pharmaceutical Manufacturing Execution Systems Conference will provide participants with an exciting and engaging platform for knowledge-share.

TOPICS TO BE ADDRESSED INCLUDE:

  • Practical approach to implementing a MES to improve efficiency, productivity & compliance
  • Efficient MES tailoring strategies to improve performance & quality in small batch manufacturing
  • Use of quality & automation standards in MES customization & continued improvement
  • Overcoming challenges in change management & the validation of an updated MES
  • Pros & cons of utilizing 3rd party integrator & future goals of MES development
  • Best practices in selecting & contracting with the right vendor for MES projects
  • Collaborating with vendors on innovative MES applications for FDA submissions
  • Practical approach to developing & implementing an MES center of excellence
  • Enhancing Electronic Batch Records design processes in pharmaceutical MES
  • Deploying the MES structure across the organization to maximize investments
  • Methods & metrics to fully comprehend the return on investment of a MES
  • Change control & change management processes for recipes & master batch records
  • Efficient means of decreasing MES selection & implementation timelines
  • Examining system integration strategies enabling a flexible & agile MES
  • Ensuring MES compliance & readiness in preparation for an FDA audit
  • Enhancing product design to reduce production errors & increase ROI
  • Overview of successful end to end, ERP, MES, & PCS implementations
  • Utilizing technology for MES: high availability, virtualization & cloud services

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