Regulatory Affairs Expertise

Tox Regulatory Advisor ApS was founded on June 1, 2009. The company focuses on Regulatory Affairs, Clinical Affairs and Quality Assurance within the Medical Device, Pharmaceutical and chemical Industries.We provide services to industry from early product development right through to product approvals and beyond. 

Our business approach is to work with our customer to navigate and set course for the companies in their compliance work. Thus, we help companies to successfully meet regulatory obligations on medical devices, medicinal products as well as chemicals and bring products to market in a time-efficient and cost-effective manner. 

Our experience spans Europe, North America, BRICS countries, Asia, Latin American Countries and Africa,

“Obtain on-demand expertise to better facilitate your business” 

Our expertise in toxicology, standards, regulatory compliance and project facilitation can bring your product and brand improved performance, and safety recognition. 

Our consultancy services can stop issues before they become problems; provide innovative solutions to complex issues, suggest processes and procedures for optimized efficiency. 

Further information regarding services, expertise and how our experience can add value to your business; please contact us at +4526709648, Email: