Looking for private QA and GMP training for your organisation?

SeerPharma can help by delivering a standard course or a customised training course tailored to your specific training needs. We offer different delivery modes too...you can host us on-site to perform in-house training or we can do virtual-classroom group training online.

Standard courses include a mix of theory and interactive workshops that address ‘real-world’ scenarios from industry. Customisation options include mixing-and-matching courses or modules from other courses and modifying workshops to case studies that are directly applicable to your operations.

Listed below are some of the most popular courses we deliver in public and private sessions.

Contact us to discuss your training needs on these or other topics and explore how we can help you.

Course Title
Good (Quality Control) Laboratory Practices (G(QC)LP / GQCLP)
Behavioural GMP – Minimising Human Error
Product Quality Reviews (PQRs)
Release for Supply (RFS) – Responsibilities of Authorised Persons (APs)
Root Cause Analysis (RCA) and Corrective and Preventive Action (CAPA)
Supply Chain Management
Quality Risk Management (QRM): Process Risk Assessment
Risk Assessment: Quality and Compliance
Cloud Computing for Life Sciences – Quality Paradigm Shift
GMP - What You Need to Know (PIC/S GMP Guide PE 009-15)
Supplier Quality Assurance (QA) – A Strategic Approach
Internal Audits – A Key to Your Quality System
Computer System Validation (CSV)
Post Market Monitoring and Pharmacovigilance
Validation – A Roadmap to Getting it Right First Time
ISO 13485 Introduction (2 half days)
ISO 13485: A Practical Approach to QMS For Medical Devices (2-days)
ISO 13485: Quality Management System (QMS) for Medical Devices Workshop (4-days)
Good Aseptic Practices (GAP)
Data Integrity (DI) – Identify and Address Your Vulnerabilities
Good Warehouse Practice
Good Writing Practices for Efficiency and Error Proofing
Annex 1 Changes (PIC/S Guide to GMP) - Manufacture of Sterile Medicinal Products
GMPs for Tissue Banks
Out of Specification (OOS) Handling
Cleaning Validation
GMP for Engineering
Contamination Control
How to Prepare for an Inspection / Audit
MTP 4.0 - Industry 4.0 for MedTech, Biotech & Pharma
ISO 14971 - Risk Management for Medical Devices

You may also interested in other SeerPharma QA and GMP Training content: