Getting drug-device combinations to market

Did you know the key to getting drug-device combinations to market compliantly is in the classification of the product? For example, establishing whether an anti-microbial component is a drug in its own right.

Download your copy of our whitepaper below…

Other key considerations are the timelines for both device and medicine, as well as meeting the safety requirements (toxicological, clinical etc.) for both and in combination.

So, what is the quickest route to market? Download our whitepaper to find out:

• How to define and classify a product
• Relevant guidance and legislation for a product
• What to expect from the regulatory pathway