That is consent; it is not implied. Written and script forms of Information Sheets must be easy to read and/or understand, be in lay language that is suitable for the participant, and capture ...

All protocols must detail the informed consent process personnel will use if participants will be involved in the research study ... Key elements: Once consent forms are approved, they will be ...

The Revised Common Rule requires all clinical trials to post an unsigned consent form on a publicly available website. The Revised Common Rule is in effect for studies approved on or after January 21, ...

The sample consent forms are being provided to you as a tool. They contain all of the required elements of an acceptable consent form. While we strongly recommend that you follow the format that we ...

It is helpful if the files are named and ordered in a logical manner (e.g. 1_smith_coverpage.docx, 2_smith_research description.docx, 3_smith_appendices, etc). Appendices materials (survey and ...

a model consent form included in the protocol and listed in the Table of Contents of the protocol with the same wording, or in the contract or agreement. An explanation of whom to contact for answers ...

See the informed consent form template (pdf) for more help and sample language. 1. Title of the Study 2 ... and their probability as a direct result of participation in the research and/or from breach ...

and involves no procedures for which written consent is normally required outside of the research context; or The subjects or legally authorized representatives are members of a distinct cultural ...

Children are persons who have not attained the legal age for consent to treatments or procedures ... in research would involve. If the research includes a wide range of ages, then multiple assent ...

The programme is being led by a dedicated Cancer Research UK funded oncology pharmacist at Guys ... oncology/haematology consultant and member of the UK SACT Board. The consent forms and guidance ...

The information and sample documents in the compliance form section are provided to help researchers develop consent and assent documents customized to the design of the individual research project.