GMP Refresher 2025

5/5
32
GMP Course - 2025 Refresher

Duration :

1

1 hour(s)

Skill level:

Regulatory

Language:

English

Final exam:

Yes

Certificate of Completion:

Yes

CEU / CPD Accreditation:

Yes

Certification:

Successful completion provides learners with a dated, traceable and downloadable certificate for the course : 

Each certificate is CPD/CEU accredited and 21 CFR PART 11 compliant. Certificates validity can be checked online through our certificate online checker. They can also be shared on Linkedin.

Description:

 Enhance your knowledge of Good Manufacturing Practices (GMP) with our GMP Refresher program. Designed for professionals in pharma, biotech, and life sciences, this course ensures you’re up-to-date with essential GMP principles, safety, and compliance to excel in regulated industries. 

 

Who should enroll?

This course is specifically tailored for professionals in quality assurance, control, and manufacturing, as well as regulatory specialists, compliance officers, and pharmaceutical managers. It provides critical insights to strengthen GMP expertise, ensure compliance, and achieve operational excellence in regulated industries.

 

Topics outlined in the course:

  • Reinforcing the principles of Quality Management for GMP compliance.
  • Best practices for Organization, Personnel, and Training.
  • Documentation and Records management essentials.
  • Core Manufacturing Operations and Control techniques.
  • Principles of Pharmaceutical Validation and process integrity.

 

This certified course integrates real-life examples and assessments to facilitate a comprehensive and applied learning experience. Upon completion, participants will receive a globally acknowledged GMP Refresher training certificate, accredited with CPD/CEU credits. 

 

Curriculum:

Introduction

Lesson 1: Quality Management

Lesson 2: Organization and Personnel in GMP

Lesson 3: Buildings and Facilities

Lesson 4: Equipment

Lesson 5: Materials Management

Lesson 6: Manufacturing Operations and Control

Lesson 7: Documentation and Records

Lesson 8: Pharmaceutical Validation

Lesson 9: Outsourcing

Lesson 10: Post Operational Activities

Lesson 11: Site and Plant Security

Lesson 12: Pharmaceutical Audits

Lesson 13: Safety and Environmental Protection

Conclusion

Evaluation

Author:

ciaran
Dr. Ciaran McEnister
Senior Pharmaceutical Executive with 25+ years of experience in medical device development. Translational Research, Pharmaceutical development, Pharmacologic/Toxicologic and Preclinical research and Regulatory compliance of small and large molecule drug candidates. Dr. McEnister has an extended experience as senior quality manager.

Reviews:

5/5
32
USD: United States (US) dollar ($) ^

$95

Buy now

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This course includes:
One-year access
Updated content every month
Certificate of completion

GxP-Training Benefits

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$95.00 / year

$95.00 / year

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