Informed consent and study conduct
Learn about the informed consent process, documentation, adverse events, and roles and responsibilities within the research team.
Barriers to completing your study
Comprehensive solutions to overcome obstacles.
Building a good research environment
This lecture discusses the requirements for setting up a good research team.
Study management checklist
This checklist will help you manage clinical studies.
Project proposal template
Use the project proposal template to submit a quotation for a clinical research related service to be delivered by your organization.
Patient information sheet and informed consent form
Use this generic template for creating a patient information sheet and informed consent form if your local ethics committee does not provide a specific template
Study binder table of contents
Use this template to create a table of contents for your study binder.
Use this delegation log template to allocate roles and responsibilities to your research colleagues within a clinical study.
Site initiation visit checklist
This checklist will help you to prepare for the site initiation visit of your clinical study.
Monitoring visit checklist
This checklist will help you prepare for a monitoring visit performed by the sponsor or a contract research organization (CRO) within your clinical study.
Site close-out visit checklist
This checklist will help you prepare for a site close-out visit performed by the sponsor or a contract research organization (CRO) at the end of your clinical study.