Which aspect is NOT typically included in a regulatory strategy?

The aspect of identifying advertising strategies is not typically included in a regulatory strategy. A regulatory strategy primarily focuses on ensuring compliance with the relevant laws and regulations governing medical devices, including understanding the specific regulatory requirements, assessing the need for submissions to regulatory bodies, and setting a timeline for approvals.

Understanding regulations is fundamental to a regulatory strategy as it guides how a device should be developed, tested, and submitted for approval. Setting a timeline for approvals is also essential, as it helps manage project milestones and align resources for compliance efforts. Assessing the need for submissions involves determining what documentation or approvals are required for a particular product based on its classification and intended use.

In contrast, advertising strategies are generally seen as part of marketing and promotional plans rather than regulatory planning. While regulatory considerations may impact how a device can be marketed, the specifics of advertising strategies fall under a separate discipline focused on market access and communications rather than regulatory compliance.