02.03.23 -- Gain Experience With Consulting & Regulatory Partners For Your Clinical Trials

As the hub of integrated regulatory workflows, Advarra eReg provides out-of-the-box integrations to centralize documents, messages, and workflows, streamlining operations inside and outside of your organization.

Companies need to speed up their current development cycle, yet there are automation gaps across the drug development lifecycle.

Bioforum offers premium medical writing services across all therapeutic areas and fields within biomedical sciences. All of our writing experts hold doctorates, and have many years of writing experience.

We are Cmed, a global CRO where technology meets expertise in oncology, cell & gene therapy, and rare disease.

Harbor Clinical’s team of GxP auditors is available to help you plan, schedule, manage, and conduct your site/vendor audits.

We support our corporate sponsors by providing both assessment and processing of SUSARS as per local and country requirements. We provide reliable reporting of adverse events, unbiased signal detection, and potential mitigation and risk management plans, based on any findings as requested. 

Florence eBinders integrates all of your clinical trial systems, automates eRegulatory processes, reduces contract negotiation time, tracks study progress, and enables secure remote monitoring on the industry-standard eRegulatory, eISF, and eSource platform.

Our team has an average of 10+ years of oncology experience and strong relationships with KOLs throughout Japan and Asia, allowing them to be on top of oncology trends.

To help sponsors, particularly those new to digital health technologies (DHTs), this guide facilitates how to use DHTs and maximize their benefits to clinical investigations.