Welcome to CDG’s Online Training Course on WHO GMP Compliance for Pharmaceuticals!

At CDG, we are dedicated to providing high-quality online training courses that empower professionals and organizations to meet international compliance standards. Our WHO GMP Compliance for Pharmaceuticals course is designed for individuals seeking to enhance their understanding of Good Manufacturing Practices (GMP) as outlined by the World Health Organization (WHO). Whether you are a pharmaceutical professional, regulatory affairs specialist, quality assurance officer, or someone aspiring to enter the industry, this course offers comprehensive self-paced learning with an online certification upon successful completion.

Why WHO GMP Compliance Matters

Good Manufacturing Practices (GMP) are essential regulations that ensure the safety, efficacy, and quality of pharmaceutical products. WHO GMP guidelines provide a globally recognized framework that pharmaceutical manufacturers must follow to prevent contamination, maintain product consistency, and comply with regulatory requirements. By adhering to GMP principles, companies can ensure public health safety, meet international regulatory expectations, and gain access to global markets.

Our course provides an in-depth understanding of WHO GMP principles, covering everything from facility design and equipment validation to raw material testing, documentation, risk management, and regulatory audits. By the end of this training, participants will have the knowledge and skills to implement WHO GMP requirements in pharmaceutical manufacturing and successfully navigate regulatory inspections.

Key Features of the Course

• Self-Paced Learning: Study at your convenience with no strict deadlines. This course is accessible 24/7, allowing you to progress at your own pace.
• Comprehensive Content: Covers all critical aspects of WHO GMP compliance, including quality control, risk assessment, validation, facility management, supplier qualification, and post-market surveillance.
• Interactive Learning Material: Engaging content with real-world examples, case studies, and quizzes to reinforce learning.
• Online Examination: After completing the course, you will take an online exam to test your knowledge and understanding of WHO GMP compliance.
• Instant Certification: Upon successfully passing the exam, you will receive a CDG WHO GMP Compliance Certificate, which can be downloaded immediately. This certification demonstrates your expertise in WHO GMP compliance, enhancing your career prospects.
• Industry-Relevant Training: Designed by experienced industry professionals and subject matter experts, ensuring practical and applicable knowledge.

What You Will Learn

This course provides step-by-step guidance on WHO GMP principles and their practical application in pharmaceutical manufacturing and quality assurance. By enrolling, you will gain a thorough understanding of:

1. WHO GMP Fundamentals

• The importance of WHO GMP in pharmaceutical quality assurance
• Regulatory requirements and their impact on global pharmaceutical trade
• Key principles outlined in WHO GMP guidelines

2. Pharmaceutical Quality Systems (PQS)

• Quality management system (QMS) requirements in WHO GMP
• Implementation of corrective and preventive actions (CAPA)
• WHO GMP documentation and data integrity principles (ALCOA+)

3. Facility, Equipment, and Environmental Controls

• WHO GMP standards for facility design, HVAC systems, and cleanroom classification
• Validation and qualification of equipment (DQ, IQ, OQ, PQ)
• Environmental monitoring and contamination prevention strategies

4. Raw Material and Supplier Compliance

• WHO GMP requirements for raw material sourcing and supplier qualification
• Raw material testing, storage, and traceability
• Control measures for excipients and packaging materials

5. Pharmaceutical Manufacturing Processes

• Process validation and in-process quality monitoring
• WHO GMP guidelines for sterile and non-sterile manufacturing
• Risk-based approaches to pharmaceutical cleaning and sanitization

6. Packaging, Labeling, and Distribution Compliance

• WHO GMP standards for pharmaceutical packaging and labeling
• Serialization and track-and-trace systems for supply chain security
• WHO GMP compliance for transportation and distribution

7. WHO GMP Audits, Inspections, and Certification

• Understanding WHO GMP audit processes
• Common non-compliance risks and how to avoid them
• Preparing for regulatory inspections and WHO prequalification

8. WHO GMP Post-Market Surveillance and Continuous Improvement

• Adverse drug reaction (ADR) monitoring and pharmacovigilance
• Product recalls, complaint handling, and corrective actions
• Continuous improvement strategies for maintaining WHO GMP compliance

Who Should Take This Course?

This course is ideal for:
✔️ Pharmaceutical manufacturing professionals
✔️ Quality assurance (QA) and quality control (QC) personnel
✔️ Regulatory affairs specialists
✔️ R&D scientists and formulation experts
✔️ Compliance officers and GMP auditors
✔️ Engineers and facility management teams
✔️ Professionals preparing for WHO GMP certification audits
✔️ Students and fresh graduates aspiring to work in the pharmaceutical industry

Benefits of Taking This Course

By completing this course, you will:
✅ Gain a thorough understanding of WHO GMP compliance and its impact on pharmaceutical quality and safety.
✅ Learn how to implement GMP principles in real-world manufacturing scenarios.
✅ Improve your career opportunities in the pharmaceutical industry by earning a recognized CDG certification.
✅ Be prepared for WHO GMP regulatory audits and inspections.
✅ Strengthen your expertise in quality assurance, risk management, and compliance.

Course Completion & Certification

At the end of the course, you will take an online exam to assess your knowledge. If you pass the exam successfully, you will receive a WHO GMP Compliance Certification from CDG. This certification can be downloaded immediately and used as proof of your expertise in GMP compliance for pharmaceutical manufacturing.

Why Choose CDG for Your Training?

• Trusted Training Provider with years of experience in regulatory compliance and industry standards
• Comprehensive, self-paced learning designed to fit your schedule
• Affordable and accessible online certification with instant download
• Industry-focused curriculum developed by GMP professionals
• No prerequisites required – suitable for both beginners and experienced professionals

Enroll Now

Don't miss this opportunity to advance your career in the pharmaceutical industry with WHO GMP Compliance certification. Gain invaluable knowledge, boost your expertise, and stay compliant with global pharmaceutical regulations.