New document explains interrelationship of all GHTF guidelines
This article was originally published in RAJ Devices
The Global Harmonization Task Force has issued a new document providing an overview of all medtech-related guidelines that have been developed by the group so far1. Its purpose is to integrate the existing GHTF guidance documents and show their interrelationships throughout the medical device lifecycle process.
You may also be interested in...
Drug companies in the EU explain how a new pilot scheme on national-level scientific advice service can benefit drug developers.
While the Dutch government negotiates an acceptable price for Leadiant Biosciences’ orphan drug CDCA, a university hospital has resumed supplying pharmacy compounded versions of the drug after addressing initial problems with the sourcing of raw materials.
The European Court of Justice has confirmed the European Medicines Agency’s approach to disclosure of data submitted as part of a marketing authorization application. It is a big disappointment for industry, which nonetheless says it supports responsible data sharing and will support efforts to develop a balanced approach.