ISPE Philippines Affiliate Members
Philippines Affiliate

Guidance Documents

  • GAMP Good Practice Guide: Enabling Innovation

    GAMP Good Practice Guide: Enabling Innovation

    Published
    The drive within life sciences to improve patient safety and product quality, and provide value to society, while reducing costs requires constant and effective innovation. However, because the pharmaceutical industry operates in a highly regulated sector, some practitioners may apply unthinking, prescriptive, and rigid approaches that are not commensurate to the needs of the process, the nature of the system, and the real risk to the product and the patient.
  • Good Practice Guide: IMP Reverse Logistics

    Good Practice Guide: IMP Reverse Logistics

    Published
    Every year the number of clinical trials conducted across the globe rises in a concerted effort to develop new or improved medicinal products that ultimately improve lives. The pharmaceutical industry has developed standards and best practices in almost every aspect of a trial. There is, however, one area that lacks foundational best practices: that of medicinal product accountability, reconciliation, and return for destruction, otherwise known as reverse logistics.
  • APQ Guide: Management Responsibilities & Review (MRR)

    APQ Guide: Management Responsibilities & Review (MRR)

    Published
    ICH Q10 sets a clear expectation regarding the role of strong leadership in terms of demonstrating and communicating “strong and visible support for the pharmaceutical quality system.” The ISPE APQ Guide: Management Responsibilities and Management Review provides a quality management framework for assessing and advancing leadership systems. It provides a systematic and proactive approach to evaluating management responsibilities highlighted in ICH Q10 as well as other key leadership components:
  • Good Practice Guide: Knowledge Management in the Pharmaceutical Industry

    Good Practice Guide: Knowledge Management in the Pharmaceutical Industry

    Published
    ICH Q10 outlines three objectives: achieve product realization, establish and maintain a state of control, and facilitate continual improvement. Embracing these objectives can be best achieved using the dual enablers, Knowledge Management (KM) and Quality Risk Management (QRM).
Management of global postapproval chemistry, manufacturing, and controls (CMC) changes is a growing challenge for industry with many issues. ICH Q12 (Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management) is a transformative document shaping...