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The Rare Disease Patients Experience
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When planning a clinical trial for a rare disease, it is important to have a holistic understanding of your patient population. You want to be aware of where your patients are coming from, and what it is like to walk in their shoes. These patients need your trial just as much as you need them; even from the earliest stages, conceptualize your rare disease trial as an altruistic relationship between the patient population and your study.
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News and Press Releases |
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Kayentis and ClinOne join forces to improve efficiency and patient experience in clinical trials
Grenoble, France, and Needham (MA), US, January 10, 2023 –
Kayentis, a global provider of electronic Clinical Outcome Assessment
(eCOA) and Decentralized Clinical Trial (DCT) solutions, and ClinOne, a
leading provider for adaptive clinical trial experiences for patients,
families and clinical sites, today announce a strategic alliance. This
collaboration combines Kayentis’ expertise in clinical trial data
collection with ClinOne’s best-in-class consent management and patient
engagement technology. Together, they enable patients and sites to
access a complete range of DCT solutions with a single point of entry
for all types of trials – from traditional to fully decentralized.
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White Papers |
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PhlexEarchive: The Right Solution for Electronic Archiving of TMF Content
Phlexglobal Ltd
Many sponsor organizations have already recognized the value of moving from paper to electronic Trial Master Files (eTMFs). But few sponsors have taken a more holistic approach to the TMF lifecycle and looked at the entire process from study start-up through archiving of the TMF in electronic format, also known as e-archiving. The recurring value of managing, tracking, maintaining and accessing electronic files should not stop at the point of archiving. All of the challenges of managing an active paper TMF carry through to a paper archive. All of the benefits of an electronic TMF also carry through to the electronic archive.
As companies look to move their compliance assets to secure, long-term storage, it is important to consider ongoing compliance requirements, security, accessibility, efficiency and costs of archiving TMF content in a digital format.
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Industry Events |
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The Pharmaceutical Manufacturing and Packaging Congress 2023 (PHARMAP 2023)
12-13 June 2023, Hilton Geneva Hotel & Conference Centre, Geneva, Switzerland
The Pharmaceutical Manufacturing and Packaging Congress 2023 (PHARMAP 2023) gathers top-level management from pharmaceutical
companies of manufacturing, primary and secondary packaging, purchasing,
and supply chain and procurement sectors, CMOs and CDMOs leaders, heads
from government and institution on 12-13, June, 2023 in Geneva,
Switzerland.
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