Neurquel is committed to upholding the highest ethical standards in clinical research, especially when dealing with conditions as misunderstood and stigmatized as hyperhidrosis. Our approach is grounded in dignity, transparency, and a shared pursuit of discovery with every participant who joins our journey.

We respect the autonomy of all participants. Informed consent is a foundational principle — no individual is ever pressured or misled. We clearly communicate all relevant details before enrollment, including potential risks, limitations, and expectations. Every participant has the full right to withdraw at any time, without explanation or penalty.

Transparency isn’t optional. We explain how participant data will be handled, stored, and used. Personal information is never sold or shared without explicit consent. Our data practices are designed to be safe, anonymized where appropriate, and strictly research-focused.

Neurquel adheres to globally recognized research ethics frameworks, including the Belmont Report, the Declaration of Helsinki, and Good Clinical Practice (GCP) standards. These guidelines shape how we design studies, collect data, and engage with the public.