All Courses

This course goes through the whole clinical trial process and also includes aspects of Good Clinical Practice and Good Documentation Practice/Essential Documents.

The course describes what investigational medicinal product sponsors, contract research organisations and clinical investigators can expect when they undergo inspection or audit.

This is a professionally developed training course which incorporates the ICH E6 R2 update implemented in June 2017, along with the new EU Clinical Trials Regulation which became live on the 31st January 2022.

This is a professionally developed, interactive and engaging online course that will provide an overview of essential documents, including which stage of the Clinical Trial process they will normally be generated.

Good Manufacturing Practice (GMP) describes the minimum standard that a medicines manufacturer must meet in their production processes.

Examines the implications of the recent General Data Protection Regulation (GDPR) that became effective on the 25th May 2018 on those working within Clinical Research.

Incorporating the new MDR and ISO 14155:2020 to develop knowledge and understanding of the Medical Devices.

CPD Points Available: 6

ISO 13485:2016 was written to support Medical Device manufacturers in designing Quality Management Systems (QMS)...

GLP regulates the practices of scientists working on the safety testing of prospective drugs.

GCLP guidance identifies the systems required and procedures to be followed within an organisation.

A short course to help with managing clinical trials during Covid-19.

This is the new updated course of GCP for 2022.

CPD Points Available: 6