Featured Articles

  1. A Blueprint For Avoiding FDA Recalls 10/9/2024

    Avoid FDA recalls and safeguard your life sciences business. Learn how QMS and EBR/eDHR solutions can prevent costly product recalls and ensure compliance with FDA regulations.

  2. Elevate Your Life Sciences QMS: 5 Must-Have Features 10/8/2024

    With advanced features and better visibility into operations, uncover how MasterControl helps organizations navigate the complexities of the life sciences industry.

  3. ICH Guidelines: Challenges And Solutions For Pharma Manufacturers 10/8/2024

    Take the next step in enhancing your pharmaceutical manufacturing processes by investing in a robust quality management system (QMS) designed for ICH compliance and operational excellence.

  4. FDA Recall Prevention: Save Time, Money, And Reputation 10/8/2024

    FDA product recalls pose significant challenges for life sciences companies. Avoid recalls with these actionable steps to mitigate risk, ensure compliance, and safeguard your organization's reputation.

  5. The State Of Digital Maturity In Pharma And Medtech Manufacturing 9/20/2024

    Explore results from a study aiming to understand why numerous companies continue to rely on manual, paper-based systems, and gain insight into how your competitors are gaining a competitive advantage.

  6. 6 Must-Haves For A Quality Management System (QMS) 9/20/2024

    Not every quality management system (QMS) has the same capabilities and connectivity. Review several features to take into consideration when selecting a QMS system for your organization.

  7. How Generative AI Streamlines GxP Compliance In Life Sciences 9/20/2024

    Generative AI is reaching a critical juncture in the life sciences industry. Learn how it is changing the game for GxP Compliance and enabling organizations to improve operational efficiency.

  8. The Importance Of Vendor And Supplier Quality Management 9/20/2024

    Explore the importance of supplier quality management, relevant standards, regulatory audits, best practices, and the overall significance of this practice within the life sciences sector.

  9. 3 Tips For An Effective Medical Device Risk Analysis 9/20/2024

    For risk analysis to be successful, it must be carried out comprehensively from beginning to end. A holistic, integrated approach is essential, along with the adoption of appropriate tools.

  10. EU To U.S. Market: Understanding 3 Core Regulatory Contrasts 9/20/2024

    Learn about three key regulatory differences between the United States and the European Union that can significantly impact the success of your market entry.