Educo Life Sciences are learning and development specialists providing technical training solutions to the pharmaceutical, biotechnology, cell & gene and medical device industries. We are focused on improving the skills and knowledge of life science professionals, so they perform with confidence, accelerate their careers and drive innovation.
Training courses throughout pharmaceutical development in key areas. Learn more about our courses on pre-clinical through to manufacturing and regulatory affairs.
Biotech or biopharmaceutical courses focused on biomanufacturing. Learn more about our training on important bioprocessing areas such as upstream processing, downstream processing and analytical studies.
CGT training or ATMP training covering regulatory, manufacturing and commercial topics. Learn more about our courses on cell therapies, gene therapies and viral vectors.
Medical device training on a range of topics including the MDR and IVDR. Learn more about our courses on regulations, quality, risk management IVDR, MDR and FDA.
We support life science leaders improve team performance by designing and delivering technical training programmes that are aligned to your teams learning requirements.
When designing training, our focus is on developing the technical knowledge and skills of individuals
The post learning implementation plan provides a framework for learners to apply what they learned in the workplace.
By having close partnerships with a range of experts we can deliver courses on any topic area.
We understand people learn in different ways. We ensure the learning approach is suitable for developing you and your team.
Educo Life Sciences supports the career development of professionals from a variety of different pharmaceutical, biotech, cell & gene and medical device companies. We work with both small, medium and large organisations from small university spin outs all the way to more established big pharma and biotech
Below is just a sample of the customers we have provided training for.
Introduction: The Role of Clinical Evidence in Medical Device Compliance In the European Union, gath...
Navigating Module 3 of the Common Technical Document (CTD) is crucial for any regulatory affairs pro...
RNA therapeutics have emerged as a pivotal innovation in modern medicine, offering targeted treatmen...