[TECH LETTER] Substance-Based Products

Manufacturers producing substance-based products need to qualify their products to be in compliance with the appropriate European legal framework.
 
This can be challenging, as depending on the mode of action and intended purpose, their product can be regulated by Directive 2001/83/EC relating to medicinal products for human use (MPD) or by the Medical Device Regulation 2017/745 (MDR).
 
In this Downloadable Techletter, we provide important information that will support you in this process.
 

GET THE TECHLETTER
Please submit the form: