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University Events
Dates
 
 
July 2023
August 2023
September 2023
October 2023
Event Type
Lecture & Seminars
Exhibitions
Open Days
December 2030
Dec
1
Lecture & Seminars
Leadership in a Digital Era
John Taylor
Room 203
09:00 UTC+0
Hall for Life Sciences
Dec
1
Exhibitions
Art for All - The Story of Public Art
Lisa Morgan
Room 102
12:00
Center for the Creative Arts
Dec
3
Open Days
All Campuses Open Day
Harlen Haynes
10:00
University Hall
Dec
5
Lecture & Seminars
The Intersection of Companies and Trusts
Emily Oconnell
Room 307
10:00
Hall for Life Sciences
Dec
6
Exhibitions
Exhibition - Black Mirror: Magic in Art
Christian Rivas
Room 108
14:00
Center for the Creative Arts
January 2031
Jan
1
Lecture & Seminars
Leadership in a Digital Era
John Taylor
Room 203
09:00 UTC+0
Hall for Life Sciences
February 2031
Feb
1
Lecture & Seminars
Leadership in a Digital Era
John Taylor
Room 203
09:00 UTC+0
Hall for Life Sciences
March 2031
Mar
1
Lecture & Seminars
Leadership in a Digital Era
John Taylor
Room 203
09:00 UTC+0
Hall for Life Sciences
April 2031
Apr
1
Lecture & Seminars
Leadership in a Digital Era
John Taylor
Room 203
09:00 UTC+1
Hall for Life Sciences
May 2031
May
1
Lecture & Seminars
Leadership in a Digital Era
John Taylor
Room 203
09:00 UTC+1
Hall for Life Sciences
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Glossary test

A caregiver plays a vital role in providing support and assistance to individuals who are unable to care for themselves due to medical conditions or disabilities. Caregivers can be family members, friends, or hired professionals who offer physical, emotional, and practical help to enhance the well-being and quality of life for those in need. Their dedication and compassion greatly contribute to the overall welfare of the individuals they care for.

Continuity of Care Records (CCR) are comprehensive documents that contain relevant patient health information, including medical history, diagnoses, medications, allergies, and treatment plans. These records are essential for ensuring seamless communication and coordination among healthcare providers involved in a patient's care. By maintaining accurate and up-to-date CCRs, healthcare professionals can deliver more efficient and effective care, reducing the likelihood of medical errors and improving patient outcomes.

A Clinical Research Associate (CRA) plays a crucial role in managing and monitoring clinical research studies. CRAs are responsible for ensuring compliance with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. They oversee the data collection process, verify the accuracy and completeness of study documentation, and ensure participant safety. CRAs are instrumental in maintaining the integrity and quality of clinical research, contributing to the advancement of medical knowledge and the development of new treatments.

A Clinical Research Study is a systematic investigation conducted to evaluate the safety, efficacy, and effectiveness of medical interventions or healthcare strategies. These studies involve human participants and aim to generate scientific evidence to support medical decisions, develop new therapies, or improve existing treatments. Clinical research studies adhere to strict protocols and ethical guidelines to protect the rights and welfare of participants and ensure the reliability and validity of the results.

Module 5 - CTAs

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DTRA 2023 Annual Meeting Logo

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Module 9 - Icon list

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Module 12 - Custom button

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1. EVIDENCE OF SUCCESS

Best practices should have measurable and demonstrable success. This dimension is meant to help teams consider whether there is a track record of successful outcomes from the use of the practice. Teams should evaluate the data to determine the fit for their situation. KPIs and tangible outcomes are at the heart of evaluating best practices for DCT.

Component 6 – 1

Priority 1: Definitions

Establish common nomenclature and definitions, archetypes, and KPIs around the practice of decentralized research.

Group 114-1

Priority 3: 
Education

Group 114-1

Priority 3: 
Education

Transparency on existing and emerging initiatives
Transparency on existing and emerging initiatives
Transparency on existing and emerging initiatives

Module 14 - Circle list

As a members-only platform, Circles offers a safe and secure space for individuals to share ideas, knowledge, and expertise without mandatory creation requirements. 
As a members-only platform, Circles offers a safe and secure space for individuals to share ideas, knowledge, and expertise without mandatory creation requirements. 
As a members-only platform, Circles offers a safe and secure space for individuals to share ideas, knowledge, and expertise without mandatory creation requirements. 

Module 16 - Card

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Helen Kirkby - Headshot
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Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industry's standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen books.

Module 18 - CTA Split + reverse option

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Check out our blog for the latest news and insights about DTRA and decentralized clinical trials. Our blog covers a wide range of topics, including industry trends, best practices, and success stories.

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Check out our blog for the latest news and insights about DTRA and decentralized clinical trials. Our blog covers a wide range of topics, including industry trends, best practices, and success stories.

Module 19 - Reports listing

Decentralized Clinical Trials (DCT) Adoption Playbook

Download Report Here

Decentralized Clinical Trials (DCT) Adoption Playbook

Download Report Here

Module 22 - Related posts

Module 30 - List

Educational Materials and E-Learning Modules

Presentations

Presentations

Educational Materials and E-Learning Modules

Presentations

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Component 7 – 1

DTRA is aligning all of the stakeholders - where everyone gets a voice. We are collectively determining what we need to do to make adoption easy and trials accessible to everyone. All of the initiatives have been driven by a diverse group of stakeholders, and the regulatory agencies have participated as well. This will give the industry a full view on what needs to happen in order to succeed and ultimately include the desired and diverse populations into clinical trials. 

Caroline Redeker, Advanced Clinical

Module 34 - PDF viewer - v1

This browser does not support inline PDFs. Please download the PDF to view it: Download PDF.