Clinical Research Associate (CRA) Training

Clinical Research Associate (CRA) Training

Download Course Summary Leaflet This interactive and engaging course was developed by industry experts with a wealth of clinical trial experience. It goes through the whole clinical trial process and also includes aspects of Good Clinical Practice and Good...
Clinical Trials Audit Preparation

Clinical Trials Audit Preparation

Download Course Summary Leaflet This is a professionally developed, interactive and engaging online course suitable for anyone working within clinical trials who wishes to gain an in depth knowledge of audits and inspections. The course describes what investigational...
GCP Refresher

GCP Refresher

Download Course Summary Leaflet This is a professionally developed, interactive and engaging online Good Clinical Practice Refresher training course which incorporates the ICH E6 R2 update implemented in June 2017, along with the new EU Clinical Trials Regulation...
Essential Documents

Essential Documents

Download Course Summary Leaflet This is a professionally developed, interactive and engaging online Essential Documents training course. It will provide an overview of essential documents, including which stage of the Clinical Trial process they will normally be...
Good Documentation Practice (GDocP) & Essential Documents

Good Documentation Practice (GDocP) & Essential Documents

Download Course Summary Leaflet This professionally developed Good Documentation Practice (GDocP) and Essential Documents course explores data integrity and document requirements in detail and demonstrates how GDocP can be implemented into a number of roles. Good...
Good Manufacturing Practice (GMP)

Good Manufacturing Practice (GMP)

Download Course Summary Leaflet Good Manufacturing Practice (GMP) describes the minimum standard that a medicines manufacturer must meet in their production processes. Compliance with Good Manufacturing Practice ensures that the medicines produced are consistent in...
Good Clinical Practice (E6 R2)

Good Clinical Practice (E6 R2)

Download Course Summary Leaflet The Faculty of Pharmaceutical Medicine has approved this course for CPD. CPD Points Available: 6 This is a professionally developed, interactive and engaging online Good Clinical Practice training course which incorporates the ICH E6 R2...
GDPR for Clinical Trials and Patients

GDPR for Clinical Trials and Patients

Download Course Summary Leaflet This professionally developed, interactive and engaging online training course has been updated for 2022! It examines the implications of the General Data Protection Regulation (GDPR) that became effective in May 2018 on Clinical...
Medical Devices

Medical Devices

Download Course Summary Leaflet The Faculty of Pharmaceutical Medicine has approved this course for CPD. CPD Points Available: 6 This is a professionally developed Medical Device training course which incorporates the Medical Devices Regulation (MDR), which became...
Medical Devices – Quality Management Systems

Medical Devices – Quality Management Systems

Download Course Summary Leaflet The publication of ISO 13485:2016 marked a turning point in Quality Management Systems for those involved in the lifecycles of Medical Devices. ISO 13485:2016 was written to support Medical Device manufacturers in designing Quality...
Good Laboratory Practice

Good Laboratory Practice

Download Course Summary Leaflet Good Laboratory Practice (GLP) regulations were developed in the late 1970s in response to malpractice in research and development activities by pharmaceutical companies and Clinical Research Organisations (CROs). GLP regulates the...
Good Clinical Laboratory Practice

Good Clinical Laboratory Practice

Download Course Summary Leaflet Good Clinical Laboratory Practice (GCLP) was first drafted and published in 2003. Then in 2006, the World Health Organisation (WHO) published GCLP guidance on its website as the standard for laboratories undertaking samples from...
Managing Clinical Trials During COVID-19

Managing Clinical Trials During COVID-19

The impact of Covid-19 for ongoing Clinical Trials could be significant and it is expected that the pandemic will interfere with the conduct of many of those Trials. The safety of study participants must be paramount, but there are also consequences for...