Multi-Regional Clinical Trials (MRCT) Website Multi-Regional Clinical Trials Website | MRCT “Information on the MRCT (Multi-Regional Clinical Trials) Center at Brigham and Women’s Hospital with four primary areas of focus that address pressing issues in multi-regional clinical trials.MRCT: About Us“”Our Focus Areas” by MRCT (https://mrctcenter.org/about/focus-areas/) is licensed under CC BY-NC-SA Read more…
MS Minority Research Engagement Toolkit MS Minority Research Engagement Toolkit – Researchers | MS Minority Research Engagement Partnership Network (MS MREPN) Tools and discussion guides, evidence-based research on patient perceptions, resources for identifying community leaders and reaching out to different groups, and educational materials. These tools are intended to help Read more…
About Page | Clinical Trials for All About Page | Clinical Trials for All A website dedicated to educating patients and caregivers about the benefits and opportunities of clinical research, including a resource library from a wide variety of national health organizations, health science companies, patient advocates, past clinical trial Read more…
Advancing Health Literacy in Clinical Research: Clear Communications for Every Participant Advancing Health Literacy in Clinical Research: Clear Communications for Every Participant | National Academy of Medicine “Incorporating health literacy best practices into materials aimed at participants is crucial for clinical research stakeholders.The highlighted website resources offer a comprehensive repository Read more…
Creating a Best Practice Template for Participant Communication Plans in Global Health Clinical Studies Creating a Best Practice Template for Participant Communication Plans in Global Health Clinical Studies | Trials ” A proposed template for universally applicable best practices in communication for clinical trial findings in low and middle-income countries. Read more…
Talking to Your Patient About a Clinical Trial Talking to Your Patient About a Clinical Trial | NIH Guidance for physicians on effectively communicating clinical trial consent to patients. Dr. Eric Kodish’s NCI-funded research introduced a sequential approach, with steps covering disease understanding, standard treatments, and clinical trial options, all Read more…
CISCRP’s Journey to Better Health Mobile Exhibit Journey to Better Health Mobile Exhibit | CISCRP CISCRP: Journey to Better Health is a model Video by CISCRP about how a mobile unit is used to provide CT education and awareness. View Here
CISCRP’s AWARE for All Program AWARE for All Program | CISCRP CISCRP: Aware for All, developed by CISCRP, stands as an exemplary educational initiative that collaborates with various organizations to disseminate comprehensible clinical research knowledge to the masses. Through this program, individuals can benefit from complimentary health screenings, interactive booths, Read more…
NIH All of Us Research Program All of Us Research Program | NIH The NIH All of Us Research Program provides an opportunity for everyone who wants to participate to provide health data to help build one of the most diverse health databases in history to help researchers learn how Read more…
Allergy and Asthma Network Trusted Messenger Community Program Allergy and Asthma Network Trusted Messenger Community Program | AAN The AAN has developed a Trusted Messenger Community Program with Sanofi that provides free online health screening, offers a six week respitory health program, and provides access to free resources. View Here
Tigerlilly Angels Program Tigerlilly Angels Program | Tigerlilly The Tigerlilly Angel Advocacy Program is model for comprehensive training in community advocacy. The Angel Advocacy Program trains women of color between the ages of 21 and 50, who have been impacted by breast cancer to become more knowledgeable about the disease Read more…
Assessing the Financial Value of Patient Engagement: A Quantitative Approach from CTTI’s Patient Groups and Clinical Trials Project Assessing the Financial Value of Patient Engagement: A Quantitative Approach from CTTI’s Patient Groups and Clinical Trials Project | Article “In a 2017 article, a novel approach was introduced for assessing the Read more…
Sponsorship Agreement Template Sponsorship Agreement Template | Template Shared by PALADIN Member Sample Sponsorship Agreement Template. Download Here
Patient Advisory Board Agreement Template Patient Advisory Board Agreement Template | Template Shared by PALADIN Member Template with contact language for individuals who participate or serves on an advisory board with language for confidentiality, data privacy, reporting, and compensation. Download Here
Services Agreement Template Between Company and Patient Services Agreement Template Between Company and Patient | Template Shared by PALADIN Member A template for an agreement between patients and an organization. Download Here
Unilateral Confidentiality Agreement Template Unilateral Confidentiality Agreement Template | Template Shared by PALADIN Member Sample template for a unilateral confidentiality agreement between a patient advocacy group and industry partner. Download Here
Discover the Tools to Support Fair Remuneration of the Patient Community for Interactions With the Pharmaceutical Industry Discover the Tools to Support Fair Remuneration of the Patient Community for Interactions With the Pharmaceutical Industry | PFMD Shares principles, frameworks, and planners for remunerating the patient community for interactions with the Read more…
Determining Fair Market Value: Demystifying the Methodology Behind Patient Renumeration Determining Fair Market Value: Demystifying the Methodology Behind Patient Renumeration | PFMD Reviews the challenges and opportunities that arise when seeking to co-create a global methodology and framework for patient FMV that is deemed fair, transparent, and ethical. View Here
International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use | ICH ICH unites global regulators and the pharmaceutical industry to develop guidelines for safe, effective medicines. Established in 1990, it has grown to include 21 Read more…
Regulations: Good Clinical Practice and Clinical Trials Regulations: Good Clinical Practice and Clinical Trials | FDA Links to current FDA Good Clinical Practice regulations governing human subject protection and the conduct of clinical trials. These materials contributed significantly to the development of the rules governing these crucial aspects of healthcare Read more…