Online Courses

This 6-hour interactive online GCP course, is designed to meet all criteria and regulatory requirements of international regulatory bodies – FDA, MHRA and EMA. Upon successful completion users are issued an individual GCP certificate recognised by sp... read more...

The Good Manufacturing Practice online training is designed as a comprehensive learning tool for professionals that need to learn about the EU Good Manufacturing Practice guidelines and regulations. The content of the course is highly interactive com... read more...

This training is based on the international regulations for Good Distribution Practice (GDP) of pharmaceutical products for human use. The training looks into the practices of wholesale distributors and the proper ways and processes concerning the di... read more...

The Good Laboratory Practice (GLP) online course focuses on the international Good Laboratory Practice guidelines. It provides full overview of the standards and requirements of regulatory authorities in regards to non-clinical studies. By taking our... read more...

The notion and definition of what “Risk” is in the context of Clinical Trials is a topic that may change in the blink of an eye, but preventing and mitigating risks is still one of the most important tasks when it comes to Clinical Research. It leads... read more...

Computer System Validation is largely used in the working structure of all life science fields. It becomes a valuable and very useful mechanism which helps the quality of performance as well production in the Pharmaceutical business. The ultimate goa... read more...

The course covers common challenging issues which audit experts and participators may face; outlines important definitions and requirements and equips with practical knowledge on appropriate methods to clinical audit execution and preparation. Additi... read more...

Clinical Data Management – the process of collection, cleaning, and management of subject data in compliance with regulatory standards.Data Management is a very crucial aspect of clinical research, explaining its burst in popularity and the pinned fo... read more...

All drug development procedures involve dealing with voluminous documentation which must include consistent, reliable and accurate data. For this reason, effective data management planning is essential to clinical studies and their appropriate conduc... read more...

This is a training the aims to help you understand the principles behind what is considered Ethical when it comes to Clinical Research. It is based on the ICH standards and specifically focuses on studies, involving Human subjects, but is not limited... read more...