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98 Drug Safety courses delivered Online
CT03a - ICH, harmonisation, and principles of Good Clinical Practice
By Zenosis
Good Clinical Practice (GCP) is a set of internationally recognised ethical and scientific quality requirements for designing, conducting, recording and reporting clinical trials. Compliance with GCP principles is required by regulatory authorities in many countries for the authorisation of clinical trials and the acceptance of their data in applications for marketing approval. The International Council for Harmonisation's guideline E6, often referred to as ICH GCP, is the international standard specification for Good Clinical Practice. In this short course we describe the ICH’s role in the harmonisation of regulations, introduce its guideline E6, and set out the principles of GCP.
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.
CT03c - Clinical trial documentation
By Zenosis
Regulatory authorities tend to abide by the maxim that ‘If it isn’t documented, it didn’t happen’. Rigorous documentation of all aspects of a clinical trial is necessary to provide evidence of GCP and compliance with regulatory requirements, as well as enabling effective management of the trial. In this short course we describe important examples of the documents designated by ICH GCP as essential to the conduct of a clinical trial.
CT03b - Clinical research teamwork
By Zenosis
A clinical trial, particularly a late-phase commercial study, is a major project requiring collaboration between the sponsor and staff or contractor, on the one hand, and the clinical investigator(s) and other healthcare professionals on the other. Good communication among all parties is essential. In this short course we introduce the major roles in a typical clinical research project and outline their duties.
Explore the intricate web of emotions, behaviors, and neurological processes underlying alcohol and drug addiction. Uncover the psychological mechanisms driving substance dependence and gain insights into effective intervention strategies. Delve into the complex terrain of addiction psychology for a comprehensive understanding of its impact on individuals and society.
GMP01d - Documentation
By Zenosis
Comprehensive documentation of procedures, formulas, work instructions, and specifications, and thorough recording of batch data, are fundamental requirements of GMP. In this short course we explain why documentation is so important, identify different types of document required, and set out some simple rules for recording and correcting data.
Paediatric Vaccination Diploma
By The Teachers Training
Specialize in paediatric vaccination with our comprehensive Diploma Course. Gain in-depth knowledge of childhood immunization schedules, vaccine administration techniques, and safety protocols. Equip yourself with the expertise to confidently advocate for and administer vaccines to pediatric patients. Whether you're a healthcare professional or aspiring to specialize in paediatrics, this course provides essential training for promoting children's health and well-being through vaccination.
Drug and Alcohol Awareness Training
By The Teachers Training
Empower yourself with essential knowledge on drug and alcohol awareness through our comprehensive training course. Learn to recognize signs of substance abuse, understand its impact on individuals and communities, and explore effective intervention strategies. Enroll now to promote healthier, safer environments and make a positive difference.
