Good Manufacturing Practice for Biopharmaceutical Manufacturing
Overview
Good Manufacturing Practice (GMP) is the foundation of effective biopharmaceutical manufacturing, ensuring adherence to stringent quality systems, regulatory standards, and contamination control measures.
This blended learning course includes interactive theory and practical, hands-on training to equip participants with the essential knowledge and skills needed to operate in a GMP-compliant manufacturing environment.
Students will develop an understanding of GMP principles, industry best practices, and regulatory expectations, enabling them to support consistent, high-quality production outcomes.
Key topics covered
- Regulatory Affairs
- Quality Systems
- Annex 1
- Quality Control
- GxP
- GDP
- Mock Inspections
- Continuous Process Verification
Who should attend
Operators, Technical Staff, New hires, Jobseekers, Sales staff, and industry employees looking to enhance their employment opportunities by increasing their knowledge of GxP in a biopharmaceutical manufacturing process.
What do Attendees Obtain on Completion?
 Attendees will receive a certificate of attendance.
Register

Course Format
Blended; Online & Onsite Training
- Two mornings of online theory
- Two days NIBRT practicals
Participants can choose to complete the full course, which includes both online theory and practical sessions, or opt for the online lectures only.
Dates & Price
Dates:
- Course 1 15/07/2025 - 16/07/2025
Online Course Only (practical sessions not included) 15 – 16 July 2025
€995.004 Places Remaining
- Course 2 15/07/2025 - 30/07/2025
Full Course: 15 – 16 July 2025 Online and 29 – 30 July 2025 Onsite at NIBRT
€2,985.008 Places Remaining