Healthcare

WHITE PAPERS AND CASE STUDIES

• Developing A Data Strategy For Clinical Trials

  This white paper outlines a standardized method for developing a data strategy that can be tailored to a company's current needs and adapted as those needs evolve.

• Filling Industry Gaps With Dedicated Cell & Gene Therapy Fluid Transfer Sets

  Read how the incorporation of transfer sets designed to support CGTs will aid in the implementation of controllable, consistent, and safe cGMP amenable manufacturing procedures.

• A Site Network’s Experience With eSource Before And During COVID

  Discover how the world's leading vaccine network adopted eSource during COVID-19 despite many obstacles that got in their way.

• Patient Diversity: Identifying Challenges, Opportunities, And Best Practices

  By listening to the voice of patient diversity and implementing FDA guidance measures, learn how stakeholders can improve trust, engagement, data reliability, patient outcomes, and promote public health.

• How MAC Clinical Research Innovates With CDMS/EDC

  Discover how a partnership with one of Europe’s largest contract research organizations exemplifies the crucial role that technology plays in the realm of clinical studies.

• Supply Chain Optimization: Investigator Sponsored Trials (IST)

  This white paper addresses the common challenges faced by biopharma organizations with regards to supply chain management and offers insight into solutions by leveraging the RTSM/IRT.

• Eliminating USP <88> In Vivo Animal Bioreactivity Testing For Polymer Characterization

  There has been growing awareness about the environmental and ethical implications of plastics used in bioprocessing. The time for a shift to well-studied, proven in vitro cytotoxicity testing is now.

• Atlantic Research Group Builds Competitive Advantage With Medrio EDC

  By using Medrio’s EDC platform, learn how Atlantic Research Group was able to achieve the flexibility needed to span multiple therapeutic areas and eliminate redundancy in documentation.

• Weighing Data Integrity: 3 Ways To Ensure Compliance

  In this paper, we will compare manual transcription to documentation with three automated or partially automated solutions, assessing the pros and cons of each.

• 8 Questions to Ask When Evaluating An MES

  Explore the purpose and value of MES solutions and walk through eight of the top questions to ask when evaluating an MES for your organization.

• Pharma Manufacturing: Top 10 Pitfalls To Avoid

  Pharmaceutical manufacturers face constant challenges and pitfalls common to the industry, but how can you avoid and overcome them to mitigate risk across the board?

• Leveraging AMI For The Low Voltage Landscape

  In this white paper, explore ways that utilities are prioritizing grid management use cases and challenges that utilities face in capturing the full value of AMI data.