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329 Courses

Diploma in Paramedicine for Paramedics - CPD Approved

5.0(2)

By Studyhub UK

Diploma in Paramedicine for Paramedics - CPD Approved
Delivered Online On Demand9 days
£399

Customer Service Level 3 Regulated with Communication Training Course

By One Education

Customer Service Level 3 Regulated with Communication Training Course
Delivered Online On Demand3 weeks
£699

Customer Service Level 3 Regulated with Communication Training Course

By One Education

Customer Service Level 3 Regulated with Communication Training Course
Delivered Online On Demand3 weeks
£699

Customer Service Level 3 Ofqual Regulated and Startup Plan Diploma Course

By One Education

Customer Service Level 3 Ofqual Regulated and Startup Plan Diploma Course
Delivered Online On Demand3 weeks
£699

Level 6 Diploma in Health and Social Care Management

4.8(12)

By Academy for Health and Fitness

Level 6 Diploma in Health and Social Care Management
Delivered Online On Demand6 days
£219

Medical Assistant Diploma - CPD Certified

5.0(2)

By Studyhub UK

Medical Assistant Diploma - CPD Certified
Delivered Online On Demand5 days
£279

Advanced Physiotherapy Diploma - CPD Certified

5.0(2)

By Studyhub UK

Advanced Physiotherapy Diploma - CPD Certified
Delivered Online On Demand6 days
£279

Anaesthetist Training

5.0(2)

By Studyhub UK

Anaesthetist Training
Delivered Online On Demand7 hours 20 minutes
£10.99

CT03e - Clinical trial investigator’s GCP responsibilities

By Zenosis

A clinical investigator is responsible for conducting the clinical trial in compliance with the study protocol, GCP, medical ethics, and applicable legal requirements. The clinical research community expects that investigators and clinical staff are fully trained in GCP. Duties and functions discussed in this short course include: provision of adequate resources; liaison with IRB/IEC; compliance with protocol; management of investigational product(s), informed consent and data records; and safety reporting.

CT03e - Clinical trial investigator’s GCP responsibilities
Delivered Online On Demand30 minutes
£25

CT03f - Informed consent in clinical trials

By Zenosis

Informed consent in clinical research is an ethical and regulatory requirement. A research subject must enter a study voluntarily, be informed about risks and benefits, and understand the difference between investigation and treatment. Subjects must not be coerced into enrolment, nor must they be enticed by exaggerated claims of benefit. Before they can enrol, all potential subjects must agree, in writing, to participate. In addition to ethical and regulatory imperatives, the potential for litigation by subjects further highlights the importance of rigorous adherence to informed consent principles. In this short course we set out the principles and requirements and provide examples of practical issues confronting healthcare professionals and subjects.

CT03f - Informed consent in clinical trials
Delivered Online On Demand15 minutes
£25