ACRP blog

AUGUST 2, 2023

Ten Ways Clinical Research Sites Can Address Their Key Challenges: Focus on the participant experience throughout the recruitment, enrollment, and retention process. Leverage data and technology to optimize participant recruitment, enrollment, and retention.

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Drug Discovery World

NOVEMBER 8, 2023

This efficiency expedites the identification of potential therapeutic targets, screening of drug candidates, and selecting eligible trial participants, all of which are crucial aspects of clinical trial design and execution. Many trials fail because they cannot enrol a statistically significant number of participants.

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XTalks

FEBRUARY 9, 2023

Medable’s DCT platform, founded in 2015, offers trial sponsors (including pharma and biotech companies) and clinical research organizations (CROs) features that include AI and machine learning-driven patient identification and site selection; digitized patient enrollment; and the ability to conduct trials in any language and country.

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WCG Clinical

JULY 25, 2023

WCG continues to make improvements to My Patient, its web-based workflow and participant management tool. These upgrades enhance efficiency, participant pathway management, and user experience. My Patient facilitates the prescreening of potential participants from all referral sources.

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pharmaphorum

JANUARY 27, 2023

These challenges pertaining to burnt-out healthcare employees have resulted in major clinical trial workflow issues, including the impact of patients’ willingness to participate in trials, and their ability to enrol. Instead, the staff is relied upon to identify this type of pertinent information. About the author Marie E.

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XTalks

JULY 29, 2021

Just as clinical researchers in other therapeutic areas have renewed their commitment to improving participant diversity in clinical trials, so too have those working in Alzheimer’s research. What Factors Promote Alzheimer’s Clinical Trial Participation? Similarly, older Latino and Hispanic individuals are 1.5

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Cloudbyz

JUNE 16, 2023

In this blog, we will delve into the overview, purpose, challenges, regulatory requirements, best practices, and digital solutions associated with clinical trial data archiving. It encompasses all forms of trial-related information, including study protocols, participant records, laboratory results, adverse events, and statistical analyses.

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Pharmaceutical Technology

JUNE 15, 2023

These trials involve screening voluntary participants and monitoring their responses. The process of drug development typically starts with the identification of a potential target for a drug. Only then does it progress to clinical trials with human participants.

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XTalks

SEPTEMBER 7, 2023

The platform is designed to support cardiologists and other clinicians in the identification, triage and diagnosis of patients. His participation in this new round could not have come at a better time.”

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Cloudbyz

MARCH 13, 2023

Data should be de-identified when possible to protect the confidentiality of the study participants. This allows for timely identification and resolution of any issues that may arise. Our innovative solution enables clinical research teams to efficiently collect, analyze, and manage clinical data of different complexity and size.

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Clinical Trials Clinical Trials Trials Compliance 52

ACRP blog

FEBRUARY 15, 2023

We must accept that the richest evidence comes from diverse trial participants, and we should not accept that a trial is of good quality if it did not have diverse enrollment. One barrier to trial participation is that people who live in remote, rural areas tend to be far from academic medical centers and other research sites.

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Cloudbyz

MARCH 25, 2021

Any life science solution built on the Salesforce platform enables a cloud based communication model for the customers, partners, and all other stakeholders. As per the IDC report worldwide semiannual software tracker report, Salesforce solutions has been ranked the leader in the global CRM landscape with ~19.8%

Clinical Trials 52

Clinical Trials Clinical Trials Trials Clinical Research 52

Cloudbyz

MARCH 25, 2021

Any life science solution built on the Salesforce platform enables a cloud based communication model for the customers, partners, and all other stakeholders. As per the IDC report worldwide semiannual software tracker report, Salesforce solutions has been ranked the leader in the global CRM landscape with ~19.8%

Clinical Trials 52

Clinical Trials Clinical Trials Trials Clinical Research 52

WCG Clinical

OCTOBER 30, 2023

4] Overweight and obesity: Self-identification as ‘overweight’ is associated with significantly higher odds of suicidality, compared to those who don’t identify as overweight. [5] Written to be as non-technical as possible, these modules are accessible to all the sites participating in a trial. 1] World Health Organization.

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Clinical Trials Clinical Trials Trials Clinical Research 59

XTalks

AUGUST 5, 2020

The use of single cell sequencing in profiling bulk, heterogeneous tissues at the single cell level can help in the identification of dominant, unique and rare cell subtypes in a sample. Chromium Single Cell Solutions. Chromium Single Cell Immune Profiling Solution. The solution can also be used to assess functionality.

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Gene Expression Development RNA Drugs 112

pharmaphorum

FEBRUARY 9, 2021

Launching a rare disease patient registry often requires patient advocacy groups to design a registry themselves or pay for an expensive customized solution. They’re best placed to co-design evidence generation solutions that are meaningful to their communities.”. Rare Central was purpose-built for patients and patient advocacy groups.

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XTalks

MARCH 20, 2024

For insights on addressing leadership-related obstacles in clinical operations, join Enciso and other esteemed professionals in the field by participating in our upcoming Xtalks Clinical Trial Leadership Peer Circle. They persistently pursue new knowledge, adapt to changes and implement innovative solutions.

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Clinical Trials Clinical Trials Trials Clinical Research 52

XTalks

MAY 11, 2023

I worked for several years at the Canadian Hearing Society, an industry-leading provider of services, products and education that empowers individuals in the deaf and hard of hearing communities to overcome barriers to participation. Webinar accessibility is not only ethical but also a sound business practice.

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Marketing Production Life Science Regulation 98

pharmaphorum

JULY 4, 2022

Together, the webinar panellists explored the potential of medical informatics solutions and methods in rare disease research, studies, data optimisation, and usability to overcome these challenges, all whilst maintaining compliance with data protection regulations and a patient-centric approach.

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Cloudbyz

MAY 5, 2023

Risk Identification The first step in RBM is to identify the potential risks associated with a clinical trial. Enhanced Patient Safety By focusing on the most significant risks, RBM can help to identify and address potential issues early, reducing the likelihood of harm to trial participants. Methodology of Risk-Based Monitoring 4.1.

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Clinical Trials Clinical Trials Trials Compliance 85

pharmaphorum

DECEMBER 18, 2020

Health inequality is the “greatest societal challenge of our time”, according to a briefing document calling for a system-wide solution. Participants heard that the health system is capturing patient ethnicity data around 65 per cent of the time.

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Development Vaccination Vaccine Research 67

pharmaphorum

JULY 5, 2022

Notable highlights include the central role the UK has played in the field of genomics, with over 500 thousand patients now in the biobank, and the recent RECOVERY trial – the world’s largest clinical trial into treatments for Covid-19, with more than 40,000 participants across 185 trial sites in the UK.

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XTalks

JULY 13, 2021

The ICH says the principles are interdependent and should be considered in their entirety to assure ethical trial conduct, participant safety and reliable trial results. With evolving technologies driving greater efficiencies and enhanced subject participation and engagement, digital oversight becomes key. Critical to Quality Factors.

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Cloudbyz

JUNE 19, 2023

Generative AI models can significantly improve this process by automating the identification and extraction of relevant information from diverse sources such as electronic health records, social media, and scientific literature. It offers 360 degree view across R&D and commercial.

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The Pharma Data

JULY 21, 2021

The trial builds on previous positive Phase 2 trials and includes both adult and pediatric participants with the aim to support acceleration of the vaccine candidate’s pediatric program. (NYSE: PFE), today announced that they have completed recruitment for the Phase 2 trial, VLA15-221, of Lyme disease vaccine candidate, VLA15.

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Vaccination Vaccine Trials Bacteria 52

XTalks

OCTOBER 12, 2022

However, the role of MRI in new drug clinical trials can involve diagnosis of lesions and determination of their severity, early identification of therapeutic responders to drug treatment and treatment monitoring and follow-up. Figure courtesy of Philips Pharma Solutions, formerly BioTel Research. DSC-MRI neuroimaging.

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Clinical Trials Clinical Trials Trials Drugs 93

WCG Clinical

MAY 24, 2023

Improving site feasibility is a complex challenge that demands a comprehensive solution. A Broken Status Quo Sponsors are stuck: The cycle times associated with study startup, including site identification and activation, have changed little over the past 20 years. Site identification and feasibility efforts begin. Some of them?

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The Pharma Data

AUGUST 13, 2020

King , the following aggregate principal amount of each series of Old Notes was validly tendered and not validly withdrawn at or prior to the Early Participation Date (as defined herein) pursuant to the Exchange Offers: CUSIP/ISIN Number. Principal Amount Tendered by the Early Participation Date. Acceptance Priority Level. 290,616,000.

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Production Sales Manufacturing Development 52

XTalks

FEBRUARY 6, 2024

Data visualization dramatically helps in the analysis and assessment with regard to the identification of potential safety signals and ensures that teams can effectively communicate any concerns ( Figure 3 ). We found that it’s important to provide practical, creative and flexible solutions to meet the needs of each patient,” Mrs. Lohr says.

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ACRP blog

APRIL 25, 2023

3 While many aspects of the clinical trial process have become more streamlined, the patient identification process still largely relies on inefficient practices. The solution runs safety rules in the background that automatically populate a safety report based on trial needs. Tufts Center for the Study of Drug Development.

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Clinical Trials Clinical Trials Trials Research 52

The Pharma Data

AUGUST 13, 2020

In accordance with the Acceptance Priority Levels and proration procedures described in the Confidential Offering Circular, Amgen will accept $676,157,000 in aggregate principal amount of the Old Notes that were tendered for exchange at or prior to the Early Participation Date. Principal Amount Tendered by Early Participation Date.

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Production Sales Manufacturing Development 52

Drug Discovery World

FEBRUARY 20, 2024

Obtaining consent from patients or healthy volunteers is a fundamental requirement for enrolling participants on to clinical trials. This can be a lengthy and complex process which must ensure participants are fully informed of all aspects pertaining to the trial. due to updated safety information or addition of new analysis.

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Drug Discovery World

FEBRUARY 20, 2024

Obtaining consent from patients or healthy volunteers is a fundamental requirement for enrolling participants on to clinical trials. This can be a lengthy and complex process which must ensure participants are fully informed of all aspects pertaining to the trial. due to updated safety information or addition of new analysis.

Clinical Trials 52

Clinical Trials Clinical Trials Trials Pharma Companies 52

Cloudbyz

JUNE 10, 2020

A patient-facing study website provides patients and participants with a comprehensive list of actively recruiting studies across different therapeutic areas and disease conditions. Prior to registration, the participant gains complete transparency of the trial and can enroll with confidence. Patient-Facing Website.

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Cloudbyz

SEPTEMBER 25, 2020

HEPAprint, MEDIKURA, Navro, Embleema & Cloudbyz develop 5 top solutions to watch out for. Our Innovation Analysts recently looked into emerging technologies and up-and-coming startups working on solutions for the pharma sector. For this research, we identified 164 relevant solutions and picked 5 to showcase below.

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Pharma Companies Big Data Drugs Clinical Trials 52

Roots Analysis

DECEMBER 29, 2023

In the past, clinical trial sponsors have shown reluctance to integrate technological solutions into clinical research, primarily, because several investigator sites still use old software and conventional techniques of data collection and reporting. It is important to note that the advantages are beyond this.

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XTalks

DECEMBER 4, 2020

Thankfully, with earlier identification and classification comes opportunity for early intervention that makes it possible to slow the progression of CKD. This development has now dramatically changed the management paradigm for this disease process. Operational Perspective of CKD Trials. Optimizing Patient Enrollment and Retention.

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