Featured Articles

  1. Celebrating Collaborative Success With 2023 CDMOs 12/19/2023

    MasterControl congratulates its customers recognized as top CDMOs in 2023. These leading organizations are driving innovation and delivering high-quality therapies through the power of technology.

  2. The 3 Stages Of MES Analytics For Drug Manufacturing 6/14/2023

    In order to access all of your organizations manufacturing data and insights, the most practical solution is a cost effective, modern MES for all lines and stages.

  3. Precision Medicine: Going Digital To Drive Innovation 6/2/2023

    The Precision Medicine Initiative is driving forward the potential for a more customized health care approach, transforming the way health care professionals are treating diseases.

  4. Solving Biopharmaceutical Manufacturing Production Records Challenges 5/30/2023

    Solve your companies manual manufacturing production records problems with modern manufacturing execution systems and gain the competitive advantage.

  5. Extending Quality Management Through Vendor Compliance Audits 5/25/2023

    Explore the primary responsibilities of both manufacturers and vendors during a vendor compliance audit, as well as practical strategies and tools, including audit management software, that make them possible.

  6. Embracing And Implementing Computer Software Assurance Guidance 5/18/2023

    Pharmaceutical manufacturers are exploring comprehensive computer software assurance (CSA) approaches, the benefits of implementing a risk-based framework, when to apply it, and the first steps to this CSA approach.

  7. Assess Your Digital Pharmaceutical Manufacturing Maturity 5/18/2023

    Learn how regulated product manufacturers are meeting the demand for faster development and delivery of products to patients and where your operations fit in the digital maturity manufacturing model.

  8. 5 Steps To Pass Your ISO 9001 Audit 5/18/2023

    Reduce your pre-audit stress and pave the way to successfully meeting ISO 9001 standards and becoming certified.

  9. Transitioning To Pharmaceutical Validation 4.0 5/16/2023

    To help companies achieve Pharma 4.0, the International Society for Pharmaceutical Engineering is driving Validation 4.0 as a way to help organizations expedite the computer software validation process.

  10. Are Electronic Manufacturing Logbooks Better Than Paper? 4/10/2023

    We accept the aid of automated paperless technology in our everyday lives, so why not in life sciences manufacturing? Check out some of the benefits of eLogbook management.