News

Jul 2023

Enhancing Clinical Trial Risk Management: A Response to the Growing Concerns over Fraudulent Studies

By |2023-07-20T12:20:47+02:00July 19, 2023|Blog, News|0 Comments

In this blog, we explore the growing concerns about fraudulent RCTs highlighted in a recent Nature article. Discover how innovative risk management approaches can detect, prevent, and tackle these issues, facilitating more robust regulatory oversight.

Jun 2023

Empowering Clinical Trials: MyRBQM Portal Debuts on Microsoft Azure Marketplace

By |2023-06-27T10:53:08+02:00June 27, 2023|News|0 Comments

MyRBQM Portal has made its debut on the Azure Marketplace. This milestone allows biopharmaceutical companies to streamline and unify their approach to risk management by using the secure and reliable Azure cloud platform.

Jun 2023

Boosting Oncology Care with Decentralized Clinical Trials

By |2023-06-06T15:11:23+02:00June 4, 2023|Blog, News|0 Comments

Discover how Decentralized Clinical Trials (DCTs) have the potential to reshape oncology care. Using our eyesON DCT Outlook, we reveal how patient demographics, broadband internet, and registered oncologists could drive DCT opportunities and potentially enhance cancer survivorship.

May 2023

eyesON | Decentralized Clinical Trials Outlook: USA

By |2023-06-21T17:28:49+02:00May 29, 2023|Interactive Data Visualizations, News|Comments Off on eyesON | Decentralized Clinical Trials Outlook: USA

Data visualization tool designed to identify untapped opportunities for Decentralized Clinical Trials advancement in the oncology sector in the USA.

May 2023

Training Implications of the ICH E6(R3) and E8(R1) Guidelines

By |2024-09-11T16:49:40+02:00May 29, 2023|Blog, Good Clinical Practice, News|0 Comments

Be prepared for ICH E6(R3): turn guidelines into real-world action. In this post, we delve into the key updates and training gaps.

May 2023

A Comparative Review of the ICH E6(R3) and E8(R1) Guidelines

By |2024-09-11T16:55:48+02:00May 26, 2023|Blog, Good Clinical Practice, News|Comments Off on A Comparative Review of the ICH E6(R3) and E8(R1) Guidelines

Unpacking the new ICH guidelines, E6(R3) and E8(R1), we illuminate their key elements, identify gaps, and compare the two in terms of their unity, differences, and complementarity.

May 2023

Embracing the Future: FDA’s New Draft Guidance on Decentralized Clinical Trials

By |2023-05-12T17:33:36+02:00May 12, 2023|Blog, News|Comments Off on Embracing the Future: FDA’s New Draft Guidance on Decentralized Clinical Trials

Dive into the FDA's latest draft guidance on Decentralized Clinical Trials and the role of Risk-Based Quality Management. Learn how RBQM and centralized monitoring can elevate your clinical research efficiency and reliability.

May 2023

Big Pharma M&As: Is It Worth the Trouble?

By |2024-06-07T14:30:31+02:00May 10, 2023|Blog, M&A Insights and Solutions, News|Comments Off on Big Pharma M&As: Is It Worth the Trouble?

Big Pharma M&As: A Worthwhile Challenge? Navigating the complex landscape of M&As in the pharmaceutical industry comes with unique objectives and potential benefits. But do these transactions truly drive shareholder value for the acquiring firm?

May 2023

Enhancing R&D Due Diligence in Pharma M&As: The Role of MyRBQM Portal

By |2024-06-07T15:19:19+02:00May 10, 2023|Blog, M&A Insights and Solutions, News|Comments Off on Enhancing R&D Due Diligence in Pharma M&As: The Role of MyRBQM Portal

Navigate your M&A journey confidently with Cyntegrity's MyRBQM Portal. Aspiring to hit your targets within 6-12 months? Discover how we can make it possible in R&D due diligence.

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