Undergraduate Certificate in Quality Certifications in Pharma Industry
-- ViewingNowThe Undergraduate Certificate in Quality Certifications in Pharma Industry is a comprehensive course designed to equip learners with the essential skills needed to thrive in the pharmaceutical industry. This course focuses on quality certifications, which are critical for ensuring compliance with industry standards and regulations.
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⢠Introduction to Quality Certifications in Pharma Industry: Overview of quality standards, regulations, and certifications in the pharmaceutical industry.
⢠Good Manufacturing Practices (GMP): Detailed exploration of GMP principles, regulations, and implementation in pharma manufacturing.
⢠ISO 9001: Quality Management Systems: Understanding the international standard for quality management systems and its application in pharma companies.
⢠ISO 13485: Medical Devices Quality Management Systems: Examination of the specific quality management system requirements for medical device manufacturers.
⢠Quality Risk Management in Pharma: Introduction to risk identification, assessment, and mitigation strategies in pharma quality management.
⢠Pharmaceutical Quality Assurance and Control: Overview of quality assurance and control principles, techniques, and best practices in the pharma industry.
⢠Pharmacovigilance and Pharmacoepidemiology: Study of drug safety monitoring, adverse event reporting, and pharmacoepidemiological research methods.
⢠Regulatory Affairs for Quality Certifications: Exploration of the role of regulatory affairs professionals in obtaining and maintaining quality certifications.
⢠Quality Audits and Inspections in Pharma: Understanding internal and external audit processes, inspection preparation, and regulatory compliance.
⢠Continuous Improvement and Lean Six Sigma in Pharma: Introduction to continuous improvement methodologies, Lean Six Sigma principles, and their impact on pharma quality and efficiency.
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