Pediatric Oncology Clinical Trials in Sub-Saharan Africa

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OCTOBER 09/2018

news roundup

TrialScope Launches Clinical Trial Transparency Service

TrialScope, a company specializing in clinical trial transparency and compliance solutions, announced the launch of its Clinical Trial Transparency Service (CTTS) for sponsors. The new service hopes to improve patient engagement, lower costs, and increase transparency through a clinical trial publication website.

Catalent Selected to Provide Oral Delivery Systems

GB Sciences, Inc. and Catalent Pharma Solutions announced that GB Sciences has selected Catalent to provide oral delivery systems, formulation development, and clinical-scale oral dose manufacturing of GB Sciences' proprietary active pharmaceutical ingredients for its Parkinson's disease therapies.

Medidata and Decibel Therapeutics Announce Multi-Year Collaboration

Medidata announced that Decibel Therapeutics is adopting Medidata Cloud and specifically using its eTMF and eCOA/ePRO solutions. The agreement will support Decibel Therapeutics' clinical development for hearing loss, tinnitus, and balance disorders.

ActiGraph Launches New Activity Monitor

ActiGraph has announced the launch of its newest activity monitor, the CentrePoint Insight Watch. This watch hopes to deliver high quality, real-world data, and an enhance patient experiences during clinical drug trials and health research studies.

In this edition

ActiGraph Launches New Activity Monitor

Comparing Risk Based Monitoring and Remote Trial Management vs. SDV

An Introduction to BYOD: What You Need to Know in a Snapshot

Pediatric Oncology Clinical Trials in Sub-Saharan Africa

Events

Rare Diseases & Orphan Products Breakthrough Summit

Basket and Umbrella Trials for Oncology

IRT 2018

eCOA / ePRO 2018

Women of Color in Pharma Second Annual Conference

2018 HBA Annual Conference

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Articles

Medical Coding Procedures in Clinical Research: An Amarex Safety and Pharmacovigilance Perspective

This article will detail how the Amarex Safety & Pharmacovigilance team performs medical coding using an internally developed safety platform.

Comparing Risk Based Monitoring and Remote Trial Management vs. SDV

A new RBM method used in PaxVax trial proves successful vs. onsite source data verification for trial oversight.

Blog Posts

An Introduction to BYOD: What You Need to Know in a Snapshot

Researchers are now looking to design their trials around a bring-your-own-device (BYOD) strategy, which allows participants in a clinical trial to provide study data using their own internet-enabled hardware.

FDA Supports Streamlined Trials for New Antimicrobials

The critical need for new medicines to combat infectious diseases is prompting FDA to join with other federal health agencies and the biomedical research community to advance the science, regulatory policies, and reimbursement strategies to promote innovation in this area.

Oncology