Executive Development Programme in PharmaTech Inspection Processes
-- ViewingNowThe Executive Development Programme in PharmaTech Inspection Processes is a crucial certificate course designed to meet the growing industry demand for experts skilled in pharmaceutical technology inspection procedures. This programme emphasizes the importance of stringent inspection processes, ensuring the highest standards of quality and safety in pharmaceutical production.
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โข PharmaTech Inspection Processes Overview: Understanding the regulatory framework, inspection strategies, and best practices in PharmaTech inspection processes.
โข Quality Management System (QMS): Implementing and maintaining a QMS in compliance with international standards and regulations.
โข Good Manufacturing Practices (GMP): Applying GMP principles in production, testing, and quality control processes.
โข Documentation and Record Keeping: Managing records, documentation, and data integrity in compliance with regulatory requirements.
โข Facility and Equipment Management: Ensuring compliance with regulations, maintenance, and calibration of facilities and equipment.
โข Change Management: Implementing change control processes, including risk assessment and validation.
โข Supplier Management: Managing suppliers and contractors, including qualification, monitoring, and auditing.
โข Deviation and Non-Conformance Management: Identifying, investigating, and resolving deviations and non-conformances in compliance with regulations.
โข Complaint Handling and CAPA Management: Managing complaints, corrective and preventive actions (CAPA) in compliance with regulatory requirements.
โข Regulatory Inspections and Audits Preparation: Preparing for and managing regulatory inspections and audits, ensuring readiness and compliance.
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