Good Documentation Practice (GDocP)

Good Documentation Practice (GDocP)

Download Course Summary This professionally developed Good Documentation Practice (GDocP) course explores data integrity and document requirements in detail and will show how GDocP can be implemented into a number of roles. Good Documentation Practice is mandatory to...
ICH GCP E6 R3 Update

ICH GCP E6 R3 Update

Download Course Summary Leaflet The upcoming release of the ICH GCP R3 signifies the commitment to continuous improvement and adaptation in the field of clinical research. Technological advancements, and how we conduct research have changed greatly over the years,...
Informed Consent

Informed Consent

Download Course Summary Leaflet This is a professionally developed, interactive and engaging, online informed consent course. This course will give you an understanding of the background and practical implications of the valid Informed Consent process. The knowledge...
Pharmacovigilance: Drug Safety and Regulations

Pharmacovigilance: Drug Safety and Regulations

Download Course Summary Leaflet This interactive and engaging course was developed by industry experts with a wealth of clinical trial and QA experience. This course provides the user with a firm understanding of pharmacovigilance and its relationship with drug...
Clinical Project Management Training

Clinical Project Management Training

Download Course Summary Leaflet This interactive and engaging course was developed by industry experts with a wealth of clinical trial experience. This course will explain everything you need to know about becoming an effective project manager within this field, from...
Good Clinical Practice (E6 R2)

Good Clinical Practice (E6 R2)

Download Course Summary Leaflet Good Clinical Practice (GCP) Course (E6 R2) The Faculty of Pharmaceutical Medicine has approved this online GCP training course for CPD points. CPD Points Available: 6 This is a professionally developed, interactive and engaging, online...
GCP Refresher

GCP Refresher

Download Course Summary Leaflet GCP Refresher Online Course This professionally developed, interactive, and engaging online GCP training course incorporates the ICH GCP E6 R2 guidance and the EU Clinical Trials Regulation which became live on the 31st January 2022....
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...
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...
Medical Devices

Medical Devices

Download Course Summary Leaflet Medical Device Online Training The Faculty of Pharmaceutical Medicine has approved this medical device training course for CPD points. CPD Points Available: 6 This professionally developed Medical Devices training course incorporates...
Good Clinical Practice (E6 R2)

Good Clinical Practice (E6 R2) – German

This is a Good Clinical Practice Course developed in English and translated into German. Kurszusammenfassung Herunterladen Die Fakultät für Pharmazeutische Medizin hat diesen Kurs für die Weiterbildung genehmigt. Dies ist ein Kurs in ‘Good Clinical Practice’,...
Good Clinical Practice (E6 R2)

Good Clinical Practice (E6 R2) – Spanish

This is a Good Clinical Practice Course developed in English and translated into Spanish. Descargar Resumen del Curso La Facultad de Medicina Farmacéutica ha aprobado este curso para CPD. Points de DPC Disponibles: 6 Este es un curso de capacitación en línea de buenas...
Good Clinical Practice (E6 R2)

Good Clinical Practice (E6 R2) – French

This is a Good Clinical Practice Course developed in English and translated into French. Dépliant de Résumé du Cours La Faculté de médecine pharmaceutique a approuvé ce cours pour le BPC. Points de DPC Disponibles: 6 l s’agit d’un cours de formation en ligne sur les...
Clinical Research Associate (CRA) Training

Clinical Research Associate (CRA) Training

Clinical Research Associate (CRA) Online Training Download Course Summary Leaflet This interactive and engaging online clinical research associate training was developed by industry experts with a wealth of clinical trial experience. It goes through the whole clinical...
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 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...
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 – 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 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...