Newsletter | June 17, 2025

06.17.25 -- Nurturing Clinical Site Relationships Drives Trial Success

SPONSOR

The PDA Regulatory Conference 2025 Achieving CGMP Excellence: Sustainable Compliance Across the Lifecycle continues its 34-year tradition of delivering impactful content that supports the development and implementation of effective quality systems across the product lifecycle. This premier pharmaceutical CGMP conference on 08-10 September 2025 in Washington, DC will focus on strategies to manage manufacturing and quality risks while driving operational excellence and sustainable compliance.

CLINICAL TRIAL TECHNOLOGY

Nurturing Clinical Site Relationships Drives Trial Success

Article | By Life Science Connect Editorial Staff

Whether a clinical trial is studying rare disease therapies or large-volume vaccines, three Ps define the approach to site feasibility: patients, product, and procedures. Advanced technological and methodological tools can assist sponsors, CROs, and sites in identifying fruitful collaborations, but person-to-person communication must drive those collaborations. 

The Catch-22 Of eConsent: A Missed Opportunity For Improved Trials

Article | Castor

Drawing on evidence from scientific literature, we examine the pitfalls that have hindered its success and propose actionable solutions to unlock its true value in clinical research.

HEOR In Action

Infographic | ISPOR—The Professional Society for Health Economics and Outcomes Research

Health Economics and Outcomes Research (HEOR) plays a vital role in guiding evidence-based decisions across the healthcare ecosystem.

How Pharma Manufacturers Can Take Control Of Their Supply Chain

Article | By Dan Cooper, Sikich

In an increasingly competitive and regulated landscape, the right ERP system is no longer optional—it’s essential to reclaim control and drive growth in pharmaceutical manufacturing.

5 Steps To Licensing Required Assessments For Clinical Trials

White Paper | By Kayla Doyle and Piero Bindi, IQVIA Technologies

Learn about the five key steps to licensing assessments for clinical trials and what to look for when choosing a vendor for your licensing needs.

Bridging The Gap Between EHR And EDC

Brochure | Medidata, a Dassault Systemes company

Clinical trial sites have long relied on manual, error-prone processes to transfer patient data from EHRs into EDC systems, but integrated solutions make streamlining this workflow quick and simple.

Optimizing The Path To RSV Vaccine Approval

Brochure | Signant Health

Vaccine trials pose unique challenges; that's why sponsors and CROs trust us to navigate complexities and capture audit-ready, high-quality evidence required to get new vaccines to patients.

Transform Your Clinical Trial Operations

Brochure | Florence Healthcare

Learn how sponsors and CROs can be empowered with this cutting-edge solution that optimizes efficiency and collaboration in clinical trial management.

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