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In the News

Pharmaceutical Outsourcing (September 2022)

Diversity In Clinical Trials Drives Better Patient Outcomes

The authors explore the latest draft guidance and review industry best practices to increase diversity in clinical trials.

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PM360 (September 2022)

Two Key Questions About Patient Experience in 2022

Soren Skovlund outlines what it takes to be a patient-first organization and how companies can better ensure they are delivering experiences that meet patients’ expectations.

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Applied Clinical Trials (September 2022)

PPD releases R&D trends in pharma and biotech report

Respondents to survey say the top challenge drug developers are currently facing is patient recruitment.

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BioPharm International (September 2022)

Robust Bioanalytical Studies Can Aid in Regulatory Submissions

Amy Lavelle discusses the challenges of performing bioanalytical studies and how CROs can help mitigate possible regulatory submission problems.

BioPharm International
CenterWatch Weekly (June 2022)

Sponsors already heeding FDA’s call for diversity planning, experts say

Rose Blackburne comments on the FDA’s guidance on trial diversity planning.

CenterWatch
Chief Learning Officer (June 2022)

Chief Learning Officer reveals 2022 LearningElite award winners

The PPD clinical research business of Thermo Fisher Scientific was named a 2022 LearningElite silver award winner for its exemplary workforce development strategies that deliver significant business results.

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Pharmaceutical Commerce (June 2022)

Positioning the patient in drug trials

The authors discuss how the clinical research industry must integrate feedback from patients and sites to eliminate unnecessary burden and accelerate enrollment in clinical trials.

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Pharmaceutical Technology (June 2022)

When is it appropriate to outsource bioanalysis work to a CRO?

Amy Lavelle and Laura Brunner discuss the factors to assess, such as type of work, regulatory considerations and the study’s needs.

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Contract Pharma (May 2022)

CRO market insights

Company thought leaders discuss the impact of COVID and regulatory frameworks for clinical trials today.

Contract Pharma