“The regulatory strategy is [part of] the corporate strategy, because without us, they can’t market in any geography,” said Susan Alpert, principal at SFA Consulting during a recent conference organized by MedTech Intelligence. In the following video, Alpert offers three key points companies should consider when building a global regulatory strategy: Go where the patients are, plan for critical markets, and know the regulatory timing based on the geography in which you’re seeking to market your product.
The 25th session of the International Medical Device Regulators Forum will be held March 11-15 in Washington, DC. The free event is open to the public and includes both in-person and virtual attendance options, Registration deadline is February 16.
The increase in global regulatory demands for medical devices has presented new challenges for regulatory affairs and intelligence teams. On May 16-17, The MedTech Regulatory Intelligence Summit will bring together regulatory professionals, device developers and regulators to look at current…
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