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Saturday, March 25, 2023
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Pharma & Biotech

Clinical Trial Management

Powering Diverse and Inclusive Clinical Trials

By Dena Raffa, Senior Director, TCN Technologies, BBK Worldwide
The Food and Drug Administration (FDA) will soon require clinical trial sponsors to submit a plan for improving diversity among clinical trial participants. While...
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Clinical Trial Management

The power of novel excipients in 505(b)(2) products

By Robert Lee, President of LLS Health, CDMO Division & Meera Raghuram, Director of Regulatory and Sustainability at Lubrizol
The FDA 505(b)(2) regulatory pathway for drug approval, which allows applicants to use existing safety data as evidence, continues to grow in popularity. Innovators...
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Clinical Trial Management

Reducing the Risk of Unintentional Unblinding

By Malcolm Morrissey, Associate Director, Statistics and Product Support Services, Sylvain Berthelot, Sr. Director, Voice of the Customer and Strategy, Calyx
Clinical trial blinding is a procedure in which one or more parties in a trial are kept unaware of which treatment arms participants have...
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Clinical Trial Management

Decentralized Centricity in Clinical Trials. What is it. How to get there.

By Oscar Segurado, Chief Medical Officer, ASC Therapeutics
The notion that a quality clinical trial should be conducted in highly specialized and experienced study centers with tight oversight of patients is becoming...
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Clinical Trial Management

Is the Burden of Clinical Trial Technology Sabotaging Sites? A Call for a Universal Solution

By Mike Wenger, Founder and CEO, VersaTrial
The ongoing digital revolution in clinical trials has created a daunting new task for the sites conducting the research: managing all the technology required...
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Clinical Trial Management

Shifting the Balance to Hybrid – Maximizing Patient Experience and Data Quality

By Caroline Jackson, Executive Vice President, Patient Services, mdgroup
Clinical trial sponsors are constantly trying to balance different goals and demands. Ensuring data quality is key, yet clients also seek to recruit diverse...
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Clinical Trial Management

Health equity movement fueled by digital innovation and disruption

By Yashoda Sharma, Program Director, Digital Medicine Society
It is not a revelation to anyone that healthcare and clinical trials have a very big problem when it comes to diversity, equity, and...
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Contract Manufacturing Organisation

The market for outsourced biologics manufacturing is expected to reach $34.1 billion by the end of 2033

Sandra Nath, Senior Contributor
Contract manufacturing organizations (CMOs) and contract development and manufacturing organizations (CDMOs) are biotechnology firms that offer a variety of services to pharmaceutical and biotechnology...
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Contract Manufacturing Organisation

Medical professionalism in a changing world

Sandra Nath, Senior Contributor
Human life was transitory before the discovery of modern medicine. Unseen risks in the form of sickness and medical disorders abound in the environment....
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Editor Picks

Image Analysis

Course Director BSc (Hons) Diagnostic Radiography and Imaging

By Clare Rainey, Course Director BSc (Hons) Diagnostic Radiography and Imaging, Ulster University 
Until relatively recently, vision had been considered an attribute of animates only.  The ImageNet challenge provided a showcase for artificial intelligence (AI) tools for...
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Clinical Trial Management

Powering Diverse and Inclusive Clinical Trials

By Dena Raffa, Senior Director, TCN Technologies, BBK Worldwide
The Food and Drug Administration (FDA) will soon require clinical trial sponsors to submit a plan for improving diversity among clinical trial participants. While...
Read more
Infection Control

Improving antibiotic use with novel diagnostic technologies: Challenges Ahead

By Matteo Bassetti , Infectious Diseases Unit, IRCCS Ospedale Policlinico San Martino
Antibiotics have revolutionized human medicine in the twentieth century. Deadly diseases such as streptococcal pneumonia or gangrene became curable, and also other advances of...
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Clinical Trial Management

The power of novel excipients in 505(b)(2) products

By Robert Lee, President of LLS Health, CDMO Division & Meera Raghuram, Director of Regulatory and Sustainability at Lubrizol
The FDA 505(b)(2) regulatory pathway for drug approval, which allows applicants to use existing safety data as evidence, continues to grow in popularity. Innovators...
Read more
Laboratory equipment / diagnostic tests

Where Is Pharma Headed in 2023?

By Keith Bowen, LES and MES Advocate_Apprentice, Apprentice
Learn 10 disruptive trends shaping the future of life science manufacturing, and how you can adapt to stay on target and ahead of the...
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Laboratory equipment / diagnostic tests

Industry Pros Come Together to Develop ASTM Protocols

By Dawn A. Lissy, Founder & President, Empirical Technologies
A powerhouse group was created with the goal of getting ASTM to adopt standards for SIJ fusion devices. Accurate, repeatable, and reproducible—that’s the mantra we’ve...
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Latest News

The market for outsourced biologics manufacturing...

Contract Manufacturing Organisation Sandra Nath, Senior Contributor
Contract manufacturing organizations (CMOs) and contract development and manufacturing organizations (CDMOs) are biotechnology firms that offer a variety of services to pharmaceutical and biotechnology...
Read more

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Constructing a Convenient Healthcare Experience

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Disrupting the Pharmaceutical Space Like Never...

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Weaving a More Informed Healthcare Space

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