Remove researcher author submit-your-paper
article thumbnail

Navigating the Global Clinical Landscape: CTA or IND for Your First-in-Human Study?

Worldwide Clinical Trials

The two regulatory frameworks offer distinct benefits and disadvantages, but which one is right for your drug development program? Once the CTA is submitted, the EU requires a new CTA for any new protocols amended. For additional insights, download our full white paper, “ First-in-Human Studies: IND or CTA? ”.

article thumbnail

UTMB and HDT Bio receive US funding for vaccine development

Pharmaceutical Technology

Optimise your cell therapy process: a guide to cell thawing. By clicking the Download Free Whitepaper button, you accept the terms and conditions and acknowledge that your data will be used as described in the Cytiva Thematic privacy policy. in milestone payments. Topic sponsors are not involved in the creation of editorial content.

Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

article thumbnail

Grand Rounds July 28, 2023: How Can Researchers Fight Misinformation About Medicine? (Carl T. Bergstrom, PhD)

Rethinking Clinical Trials

Bergstrom, PhD Professor, Department of Biology University of Washington Slides Keywords Research, Misinformation, Media, Social Media Key Points Misinformation abounds in medicine and about medicine. As researchers, we are producers and consumers of the medical literature. Researchers need to understand how preprints are received.

Medicine 130
article thumbnail

Are your food containers as healthy as your food? Participate in the Survey!

Sciensano

Reducing packaging waste without compromising safety is possible thanks to your contribution! FCM can be constructed from a wide variety of materials like plastics, rubber, paper and board, metals and alloys, ceramics, but also the printing inks and adhesives used on the outside of the packaging. Participate in the survey!

article thumbnail

Regulatory and Ethical Considerations for eConsent in Research

Advarra

In the last few years, the clinical research industry has seen a bigger push for electronic informed consent (eConsent) than ever before. eConsent can include something as small as research staff collecting an eSignature via PDF, or as large as using a comprehensive eConsent platform. These parameters are broad and vague.

article thumbnail

Advancing Medical Record Management: The Power of AI/ChatGPT

XTalks

This inefficient system is heavily based on paper records and is putting healthcare providers at a significant disadvantage. Moreover, paper medical records occupy valuable storage space in hospitals and offices. Additionally, paper records are prone to irreversible damage. This is up from 24.1 days in 2017 and 21 days in 2004.

Doctors 97
article thumbnail

MIT Researchers Create AI that Detects COVID-19 Infections Through Cellphone-Recorded Coughs

XTalks

MIT researchers developed an algorithm that has correctly identified asymptomatic people with COVID-19 by the sound of their forced coughs using their smartphone devices. The researchers have found that asymptomatic people may differ from healthy people in the way that they cough. Related: Can Dogs Identify COVID-19 Positive People ?

Research 126