Newsletter | February 20, 2019

02.20.19 -- Top 5 Strategies To Execute And Document GCP/GVP Vendor Oversight

Featured Editorial
Top 5 Strategies To Execute And Document GCP/GVP Vendor Oversight
By Penelope Przekop, MSQA, RQAP-GCP

Over the last 10 years the face of clinical R&D and pharmacovigilance (PV) outsourcing has dramatically changed. What was a common industry scenario by 2010 — a full-scale operational pharma company utilizing both international and U.S.-based CROs to execute clinical investigator site monitoring and data management — has evolved into a new common scenario in 2019.

Digital Platforms For Patient Engagement In Clinical Trials: Trends And Outlook
By Mathini Ilancheran, principal analyst, R&D, Beroe Inc.

Pharmaceutical companies have three targeted users: physicians, pharmacists, and patients. Various digital platforms are used to create a good customer experience for educating these end users. The core focus is on patients driving patient care, education, and adherence.

Industry Insights
Disrupting Clinical Operations With CRO Strategic Partnerships
Article | By Craig Morgan, goBalto

With most sponsors utilizing an outsourcing model of some kind, the biggest opportunity might still lie ahead. As the industry adapts to be more budget-minded and efficient, the quest for innovation remains. So, what does meaningful innovation look like for the clinical trial industry?

The Challenge With Early-Phase Oncology Trials
Podcast | Worldwide Clinical Trials

Less than 10 percent of oncology patients actually participate in clinical trials. How can a trial be easy or effective if patient participation is low? Get the tips you need to run better early-phase oncology trials now.

Protein Therapeutics By Immunoaffinity LC-MS: Latest Trends And Recommendations
Webinar | Q2 Solutions

Learn about the application of immunoaffinity LC-MS to regulated bioanalysis of biotherapeutics.

How Linear Clinical Research Accelerated Trials Timelines And Improved Global Collaboration With eSource
Webinar | Medrio

Explore the ways Medrio eSource has enabled Phase 1 clinical research unit to improve global collaboration and accelerate trial timelines.

Navigating The Complexities Of NASH Development: Valuable Insights From A Key Opinion Leader
Webinar | Medpace

In this webinar, medical and operations experts from Medpace facilitate a Q&A session with Dr. Stephen A. Harrison, an experienced key opinion leader (KOL) in NASH. The presenters participate in an in-depth discussion on selected topics associated with NASH development as well as strategies and opportunities for researchers.

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