Rules are rules, but are they always necessary? Short answer: Yes!
Comprehensive regulation and standards have reshaped the medical device and drug landscape by improving the efficiency of the product development process. They ensure your product functions according to its intended use and keep the end-user safe.
Following regulations/standards and having a robust QMS, cuts down on manufacturing delays and product recalls, saving you time and money.
In this free webinar presented by Isabella Schmitt RAC, Director of Regulatory Affairs at Proxima Clinical Research, you will learn how regulations, standards, and a QMS all come together to create a better, safer product and improve your bottom line.
Check out the replays of this webinar, here.