Remove Clinical Research Remove Clinical Trials Remove Licensing Remove Research
article thumbnail

Breaking Barriers: Reasons to Expand Site Cancer Clinical Trial Portfolios

WCG Clinical

In this article, we will explore the significant value derived from conducting clinical trials sponsored by pharmaceutical companies for both physicians and hospital systems, with a specific focus on cancer care, and address potential counterarguments.

article thumbnail

Licensing regime posing challenge to micro and small medical devices industry: SMTA

AuroBlog - Aurous Healthcare Clinical Trials blog

The Central government’s actions to mandate licensing of all medical devices is posing a challenge to the industry, especially the micro and small enterprises in the sector, says the Surgical Manufacturers and Traders Association (SMTA), the pan India organisation of manufacturers and traders of surgical equipment for healthcare services providers (..)

Licensing 169
Insiders

Sign Up for our Newsletter

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

article thumbnail

Psychedelic clinical trials: What sponsors should know when designing new protocols

Worldwide Clinical Trials

BioPharma Dive interviewed our Christine Moore on how to conduct psychedelic clinical research. With regulators and lawmakers seemingly on board, sponsors have more opportunities than ever to pursue clinical research in this high-velocity area. Managing the ethics of psychedelic trials. billion in 2027.

article thumbnail

Importer of Record for Clinical Trials

Imperical Blog

Avoiding “Customs Chaos” in Clinical Trials Means Working Closely with Your Importer of Record Many global clinical trial shipments get muddled regarding the critical role and responsibilities of the importer of record (IOR) for clinical trials.

article thumbnail

Importer of Record for Clinical Trials

Imperical Blog

Avoiding “Customs Chaos” in Clinical Trials Means Working Closely with Your Importer of Record Many global clinical trial shipments get muddled regarding the critical role and responsibilities of the importer of record (IOR) for clinical trials.

article thumbnail

Transforming Clinical Trial Management: The Shift from Point Systems to Platform Solutions

Cloudbyz

The landscape of clinical trial management is undergoing a significant transformation, driven by the complex demands of modern medical research. As we delve into the challenges posed by point systems, it becomes clear that a platform approach is not just beneficial but essential for the future of clinical trials.

article thumbnail

The Regulatory Binder Checklist For Clinical Trial Sites

Advarra

A regulatory binder is essential for managing clinical trial documents, ensuring regulatory compliance, and facilitating audits. It organizes critical documents; provides easy access for trial monitors, auditors, and regulatory authorities; and serves as a reference for the research team.