Newsletter | May 22, 2025

05.22.25 -- How To Pick The Perfect Clinical Trial Partners

SPONSOR

Webinar: How Sponsors can leverage site technology to standardize quality and improve site performance

With Central eSource, sponsors define a standard electronic source template, pre-map it to the eCRF, and send it to sites, where it can be configured locally to reflect their SOPs. Learn how sponsors can leverage the electronic source trend to accelerate site startup, standardize data quality at the point of capture, accelerate EDC entry, and enable true centralized remote monitoring.

OUTSOURCING MODELS

When To Outsource — And How To Pick The Perfect Clinical Trial Partners

EMED Technologies Director of Clinical Affairs Alex Nikanorov shares the company’s approach to deciding which clinical research functions to outsource and finding vendor partners that align with the company’s goals.

Choosing A Digital Health Sensor Partner In Clinical Trials

Explore what your organization should consider when selecting a digital health partner and monitoring solutions for your clinical trial.

Non-Clinical vs Clinical: Developing Modified Release Dosage Forms

Explore case studies to describe the specialized formulation technologies that are available in the “toolbox” to achieve an optimal target product profile.

Delivering Specialist Neurology Support

Explore a strategic approach to a Parkinson’s disease trial that leveraged a global infrastructure and multilingual workforce to provide seamless operational and clinical support.

Delivering High-Quality Trials With Expert Consultation In Cancer Research

The rapidly evolving landscape of oncology clinical trials, driven by innovative technologies and deeper insights into cancer biology, presents unique challenges and opportunities for U.S. biotech companies.

Bioanalysis Solutions

Learn how a bioanalytical testing partner with comprehensive solutions and unwavering commitment to quality can help you bring safe and effective drugs to market with confidence.

Altasciences' Facilities Moving In Unison

With nine facilities across North America, explore our integrated, comprehensive solution for all your early-phase drug development needs and unique expertise.

REGULATORY & COMPLIANCE

U.K. Has Strong Plan To Reform Clinical Trials

The U.K.’s 2025 clinical trial reforms aim to boost research efficiency, inclusivity, and global competitiveness by streamlining approvals, enhancing patient involvement, and addressing structural, demographic, and therapeutic gaps in trial activity.

GxP Audits Guide For Successful Clinical Trials

This step-by-step guide helps sponsors and sites prepare for and navigate the various types of audits required at each stage of the clinical trial process.

Successful Regulatory Submission Via The Trifecta Of Awesomeness

Three essential elements contribute to a repeatable, adaptable regulatory submission process: strategic planning, team engagement, and properly leveraging team experience.

Multi-Regional Clinical Trials: The Latest Guidance From FDA

Conducting multi-regional clinical trials (MRCTs) is essential for accelerating oncology drug development and ensuring broader patient access. However, differences across regions can impact findings.

CHOOSE YOUR OWN ADVENTURE

You're receiving the Thursday edition of the Clinical Leader newsletter, focusing on Outsourcing Models and Regulatory & Compliance. To make changes to your newsletter selections, update your topic preferences.

  • Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
  • Clinical Trial Technology (Tuesday)
  • Decentralized Trials | Trial Management (Wednesday)
  • Outsourcing Models | Regulatory & Compliance (Thursday)
  • Clinical Data Management & Analytics | Trial Monitoring (Friday)

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