Pharmaceutical and biotech manufacturers must ensure compliance to ICH GMP. As part of this, manufacturers must demonstrate their employees are knowledgeable and up to date with the latest GMP requirements. the best way to do this is with regular GMP training.
We provide a range of enterprise solutions in GMP and GDP to suit your requirements from bespoke customised in-person training to online on-demand licenses. Our courses are designed and delivered by a faculty of GMP experts. To meet your specific training requirements we apply a flexible and adaptive approach.
Our range of GMP courses are listed below. All courses can be customised to meet your learning and delivery requirements. The GMP training programmes can be delivered in-person (classroom), live online or on-demand.
Find a course relevant for your team and get in touch. We recommend a short consultation with our team to discuss your requirements.
Overview: This online training is designed to provide a broad overview of GMP. It introduces key concepts and explains why GMP is so important in pharmaceutical manufacturing.
Who: It is designed for all professionals that work in a GMP environment from technicians to warehouse staff.
Overview: This online course examines GMP requirements for technical staff who are responsible for manufacturing the product. It is a follow on from the foundation training course.
Who: It is designed for more technical professionals working in a GMP such as QA, QC and validation.
Overview: This online training is designed to provide a complete overview of GDP. It introduces key concepts of Good Distribution Practice and explains why it must be followed.
Who: It is designed for all professionals that work in a GMP environment from technicians to warehouse staff.
Either delivered in-person or as a live online, this training option is fully customised to meet your specific needs. We design the course to incorporate your products, technology, processes and SOPs.
This training programme will teach you strategies, tools and techniques to identify, manage and mitigate errors. Designed for quality team leaders, it will support with skills in motivating and driving a cultural change to ensure a more efficient and cost-effective approach to GMP.
Data integrity has been a focus for pharmaceutical regulatory inspections for several years. This data integrity training course will provide you with the knowledge and practical skills to implement data integrity best practice.
Effective root cause analysis is both a regulatory expectation and a valuable tool for business improvement. This training course will provide you with a range common tools used during root cause identification such as brainstorming, Ishikawa diagrams and process maps.
Overview: Our online training is designed provide an overview of ISO 13485. It introduces key concepts and explains why the quality management system is critical in medical device manufacturing and development.
Who: It is designed for all professionals that work in a medical device ISO 13485 environment from engineers to warehouse staff.