Central Laboratories Featured Articles
-
AI In Drug Discovery And Development — Will It Live Up To The Hype?
1/5/2024
While AI may soon transform the drug discovery and development process, there are still several barriers, both technical and ethical, to the rise of AI in biopharma.
-
What Clinical Trial Experts Think Will Happen With AI In 2024
12/26/2023
In part one of this preview of clinical trials trends for 2024, experts discuss the applications of AI in clinical research.
-
WHO's 6 Principles For An AI Regulatory Framework For Medical Product Development
12/14/2023
In mid-Oct. 2023, the WHO published a paper titled Regulatory Considerations on Artificial Intelligence for Health, identifying the key principles that international regulatory frameworks for artificial intelligence (AI) should address and are, in fact, starting to coalesce around. The paper was developed in consultation with a WHO Working Group whose members include regulatory authorities, policy makers, and more.
-
Pacesetters Are Product Innovators Who Embrace Digital Process Enhancement
12/12/2023
The Josh Bersin Company recently underwent research examining pharma/biotech “pacesetters” in the field. We caught up with Jordan Schmitting, senior research analyst at The Josh Bersin Company, to discuss the trends illuminated by the research.
-
Can Data Help Improve Diversity In Clinical Trials?
12/7/2023
Denise Bronner Ph.D., director of diversity, equity, and inclusion in clinical trials at Johnson & Johnson Innovative Medicine (JJIM) talks about some of the types of datasets that can be leveraged to improve diversity in clinical trials.
-
Bayesian Adaptive Designs in Clinical Trials: Using Data Science To Optimize Investigational Product Supply
11/30/2023
While it is challenging to make precise predictions for clinical trial supplies, applying Bayesian statistics will help. This article shares steps to plan your Bayesian approach and how it helps to reduce waste and prevent shortages.
-
5 Habits For Ship-Shape Source Data
11/28/2023
ALCOA+ — or Attributable, Legible, Contemporaneous, Original, and Accurate + Complete, Consistent, Enduring, and Available — is the basis for these must-follow tips from Moderna Senior Manager of R&D Quality Kaitlin Bova.
-
An Overview Of FDA Efforts To Encourage DHT Use In Drug & Biological Product Development
10/30/2023
The FDA issued its Framework for the Use of Digital Health Technologies in Drug and Biological Product Development earlier this year, representing the agency's road map on the topic. Digital health technologies (DHTs) may include wearable, implantable, or software applications, among other approaches. This article takes a closer look at the framework as well as related FDA efforts this year.
-
Key Considerations For Cell & Gene Therapy Developers To Tap Into AI
10/24/2023
In the authors' first article in this two-part series, they discussed the opportunities for AI to assist cell and gene therapy companies. In this second article, they examine how cell and gene therapy developers can wisely harness AI, with a look at outsourcing vs. developing in-house solutions, data acquisition strategies, the three stages of managing AI/ML algorithms, and more.
-
How To Balance Data Privacy And Sharing: A New Methodology For Clinical Data Reuse
10/18/2023
The TransCelerate BioPharma consortium is proposing a new methodology to enable secondary use of primary health data. Included are best practices that help increase transparency around the privacy safeguards used on trial data, increase data utility for the reuse of existing trial data, and protect patient privacy.