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Why a Platform Approach is Vital for Clinical Research Management Transformation

Cloudbyz

The clinical research landscape is rapidly evolving. As it becomes more complex with growing volumes of data, evolving regulations, and the pressure for faster drug development, traditional methods of clinical research management are no longer sufficient. Improved Scalability As research organizations grow, so do their needs.

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Beginner’s Guide to 21 CFR Part 11 Compliance

Advarra

One way to do so is to ensure the software platforms you are using to conduct research are in line with federal regulations. While Part 11 is widely known, this blog explains how it fits in with your research software. In 1997, FDA released regulations providing guidance on the use of electronic systems.

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Accelerating Consumer Product Research with Unified Clinical Trial Management Solutions

Cloudbyz

The pursuit for the most effective and safe products requires rigorous clinical research, which involves meticulous trial design, recruitment, data collection, and subsequent analysis. Let’s delve into how these solutions can accelerate research and bring products to market faster.

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Can Natural Food Dyes from Cabbage Replace Synthetic Options?

XTalks

New research published in Science Advances has suggested that a natural cyan blue extracted from red cabbage could replace synthetic blue dyes in food. Food coloring is an essential part of the food and beverage industry; however, some research suggests that using synthetic dyes is not healthy for the consumer. 1, FD&C Blue No.

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New IFPMA and EFPIA guidance on use of social media by the pharmaceutical industry

pharmaphorum

Discussion Forums – If discussion forums are hosted or facilitated by a company, the company should be confident it can moderate the forum such that the content complies with relevant regulations, laws, and codes. Why is guidance needed? What are the rules on Social Media Influencers and Digital Opinion Leaders?

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Q&A: The IND Journey Phase I – Navigating Success

Advarra

If you mean using a different contract research organization (CRO) for the different phases of clinical trials – that’s different. The standard for the audit used depends on the type of vendor and would include the applicable regulations and ICH guidelines. The sponsor is the pharmaceutical company conducting the trial.

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25 Reasons Why Pharmaceutical Companies Need a Unified Clinical Trial Management Platform

Cloudbyz

Enhanced Collaboration: A unified platform fosters better communication and collaboration among research teams, sponsors, investigators, and other stakeholders. This blog explores 25 compelling reasons why pharmaceutical companies should adopt such a platform to streamline their clinical trial operations.