Graduate Certificate in Compliance and QA in Pharma
-- viewing nowThe Graduate Certificate in Compliance and QA in Pharma is a comprehensive course designed to meet the growing industry demand for professionals with expertise in compliance and quality assurance. This certificate program equips learners with critical skills necessary to ensure adherence to regulatory standards, maintain quality control, and drive continuous improvement in pharmaceutical production and distribution.
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Course Details
• Regulatory Compliance in Pharma: Understanding FDA regulations, ICH guidelines, and other global pharma compliance requirements
• Quality Assurance (QA) Principles: Implementing QA systems, GMP (Good Manufacturing Practices) compliance, and quality risk management
• Pharmacovigilance: Adverse event reporting, pharmacovigilance systems, and pharmacoepidemiology
• Clinical Trials Compliance: ICH-GCP (Good Clinical Practice) guidelines, informed consent, and clinical trial monitoring
• Data Integrity in Pharma: Data governance, data life cycle management, and ALCOA+ principles
• Quality Control (QC) Strategies: Quality control tools, statistical process control, and SOPs (Standard Operating Procedures)
• Auditing and Inspection Readiness: Conducting internal audits, mock inspections, and responding to regulatory authority inspections
• Pharma Supply Chain Management: GDP (Good Distribution Practices), supply chain security, and cold chain management
Career Path
Entry Requirements
- Basic understanding of the subject matter
- Proficiency in English language
- Computer and internet access
- Basic computer skills
- Dedication to complete the course
No prior formal qualifications required. Course designed for accessibility.
Course Status
This course provides practical knowledge and skills for professional development. It is:
- Not accredited by a recognized body
- Not regulated by an authorized institution
- Complementary to formal qualifications
You'll receive a certificate of completion upon successfully finishing the course.
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