Featured Articles

  1. Do You Have an FDA Audit Process in Place? 2/23/2023

    Ease the stress of a U.S. Food and Drug Administration (FDA) visit to your facility by learning how to maintain a state of FDA audit process readiness.

  2. How To Solve Difficult Challenges Of Cell&Gene Therapy Manufacturing 2/17/2023

    Explore how paper batch records hold back cell and gene therapy manufacturing and the digital solutions that could help improve efficiency.

  3. 3 Steps To Achieve Total Quality Management In Pharma Manufacturing 2/17/2023

    How can your company capitalize on the latest quality management trends by adding Total Quality Management tools to their toolboxes?

  4. The 7 C's Of A Compliant Manufacturing Change Control System 2/8/2023

    Change control is integral to continuous quality improvement and customer satisfaction. Learn about the manufacturing change control process, its requirements, and the characteristics a change control system should possess.

  5. 3 Reasons To Invest In Truly Paperless Manufacturing 2/8/2023

    Learn how going paperless on the production floor can produce measurable results that have a significant impact on manufacturing operations, product quality, and the bottom line.

  6. FDA Remote Inspections Guidance 2/8/2023

    Since the COVID-19 pandemic first hit, remote audits and inspections have been essential. Learn about remote audits and inspections and how audit management software can make the process easier.

  7. Quality Management Process Improvement 2/7/2023

    With the constant introduction of new technologies, employees are regularly overwhelmed by organizational complexity and information overload. Learn how to achieve simplicity in quality management, facilitate change, and more.

  8. 3 Steps To Developing Adaptability In Pharma Supply Management 1/23/2023

    Explore three practical steps pharma manufacturers can take today to start modernizing and streamlining their pharma supply management activities and to keep up with new approaches to supplier management.

  9. Adopting A Quality Management Maturity Model In Drug Manufacturing 1/11/2023

    The objective of QMM is to elevate quality beyond the base level of cGMP. Explore practical paths to pharma QMM and the key benefits of a digital pharma QMS.

  10. Key Strategies For MES Software Integrations 1/4/2023

    To stay competitive in an increasingly dynamic field, pharma and biotech manufacturers are implementing numerous beneficial technologies to automate and streamline production. Explore the power of MES integration.