Video: An overview of FDA’s premarket regulation of medical devices
FDA’s legal and regulatory framework The definition of a medical device FDA’s risk-based classification of a device...
Biopesticides, Plant Growth Regulators, and Biostimulants: 5 questions about the US regulatory framework answered
TSG Consulting recently hosted a panel discussion exploring the process of registering new products in these...
Analysis of the US FDA’s draft guidance on nitinol-containing medical devices
Senior Regulatory Consultant, Dr. Om Singh, was published in the February 2020 issue of the Journal of Medical Device...
BPR: 5 steps to correct substance ID
The significance of correct substance identification under the Biocidal Products Regulation (EU) No. 528/2012 (BPR) is...
REACH: Brexit Q&A
Brexit is a fast-moving subject that will have regulatory and commercial implications for chemical companies with an...
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