Harold D Stowe, BS

Regulatory Consultant


+1 202 828 8964 [email protected]

Harold “”Hal” Stowe is a Regulatory Consultant supporting clients achieve pre-market and ongoing compliance with US FDA and EPA federal regulation.

Hal supports both start-ups and multi-national companies in the development and execution of strategies to navigate FDA’s premarket authorization pathways for medical devices and combination products – including 510(k) Premarket Notification, De Novo Review, and Premarket Approval applications (PMA).

Hal assists clients with receiving FDA feedback on a variety of actions:

  • Investigational Device Exemptions (IDE)
  • Pre-Submissions
  • 513(g) Requests

Hal also specializes in pre- and post-market compliance for chemical and mechanical antimicrobial technologies under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA).

Hal has a Bachelor of Science in Economics, and Bachelor of Science in Agribusiness from Clemson University.

Haven't found what you were looking for?

Servicesarrow pointing right

We help companies navigate the regulatory landscape across a range of geographies and jurisdictions. Read about the comprehensive range of services we offer.

Regulatory advicearrow pointing rightarrow pointing right

With offices throughout the US and Europe, we can help you with navigating the complex, global regulatory environment.