Global Certificate in GMP Compliance Documentation
-- ViewingNowThe Global Certificate in GMP Compliance Documentation course is a comprehensive program that emphasizes the importance of Good Manufacturing Practices (GMP) in the pharmaceutical, medical devices, and food industries. This course is designed to meet the growing industry demand for professionals who can ensure compliance with GMP regulations and document procedures effectively.
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โข Introduction to GMP Compliance Documentation: Understanding GMP (Good Manufacturing Practice) compliance and its significance in the pharmaceutical and healthcare industries.
โข Regulatory Framework for GMP Compliance: Overview of global regulatory bodies and their guidelines for GMP compliance, such as FDA, EMA, and WHO.
โข Documentation Control: Best practices for creating, reviewing, and approving GMP-compliant documentation, including SOPs, work instructions, and training records.
โข Quality Management Systems (QMS): Implementing and maintaining a QMS in alignment with GMP compliance requirements.
โข Change Management: Managing changes in GMP-compliant environments, including risk assessment, implementation, and validation.
โข Deviation and Non-Conformance Management: Identifying, investigating, and resolving deviations and non-conformances in GMP-compliant settings.
โข Corrective and Preventive Action (CAPA): Implementing CAPA processes to address and prevent recurrence of deviations and non-conformances.
โข Validation and Qualification: Understanding and executing validation and qualification processes for equipment, facilities, and systems in GMP-compliant environments.
โข Audit and Inspection Preparedness: Preparing for and managing internal and external audits and inspections in GMP-compliant settings.
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