Global Certificate in PharmaTech Auditing Standards
-- viewing nowThe Global Certificate in PharmaTech Auditing Standards course is essential for professionals seeking expertise in the pharmaceutical technology industry. This course focuses on providing learners with a deep understanding of current auditing standards, ensuring compliance with regulations, and minimizing risks in pharmaceutical technologies.
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Course Details
• PharmaTech Auditing Standards: An Overview
• Global Regulatory Framework for PharmaTech Auditing
• Quality Management System (QMS): ISO 13485 & 21 CFR 820
• Good Manufacturing Practices (GMP) & Good Laboratory Practices (GLP)
• Risk Management in PharmaTech Auditing: ISO 14971 & ICH Q9
• Data Integrity & Documentation Control in PharmaTech Auditing
• Auditing Techniques & Best Practices
• PharmaTech Auditing: Root Cause Analysis & CAPA
• Sterile Processing & Cleanroom Standards in PharmaTech Auditing
• Supplier Auditing & Quality Agreements
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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