How to Select the Right eTMF System and Vendor
Managing your Trial Master File (TMF) is a necessary, and ...
Felix Arellano
Global Head of Drug Safety – Roche
Hans van Leeuwen
Global Head of Regulatory Operations – Astellas
Julie Thomas
Vice President, Global Medical Safety Operations – Johnson & Johnson
Managing your Trial Master File (TMF) is a necessary, and ...
Our VP of Safety, Beena Wood, shares the power of ...
Our Director of Product Marketing - Clinical, Art Brown, shares ...
Identification of Medical Products (IDMP) has been harmonizing data globally ...
Advances in clinical trial design and technology are significant contributors ...
Robin Schilling, Product Manager for LifeSphere IDMP, discusses the core ...
Modernization is critical to enhance patient experience and boost clinical ...
The public is more aware of drug safety and health ...
DCTs completely revise historical trial processes by executing trials through ...
Managing the submission of medicinal products, medical devices, and biologics ...
ArisGlobal is a pivotal partner in the life sciences industry, specializing in solutions that drive drug development, safety monitoring, and regulatory compliance. We collaborate with more than 500 global life sciences companies, CROs, and government health authorities, including leading biopharmaceutical firms and regulatory bodies such as FDA, Health Canada, and NMPA.
Headquartered in the United States, ArisGlobal has regional offices in Europe, India, Japan and China.
Quick Links
© 2024 ArisGlobal – All Rights Reserved