Question 1

We don't need an alternative to the FDA.

Accepted Answer

Patients seeking experimental therapies know the FDA is too slow, and the FDA itself has acknowledged that current regulations are onerous, unnecessarily demanding, and stifle innovation. Accepting the status quo pushes America's most cutting-edge biotech companies overseas.

Question 2

Drugs not approved by the FDA are dangerous and exploitative.

Accepted Answer

Patients remain protected by statutory guardrails, state DHHS regulation, medical malpractice liability, and professional licensing. IVF and Lasik are regulated as the practice of medicine under state frameworks rather than the FDA's phased trial regime, and neither is a 'Wild West' for patients.

Legalize Cutting-Edge Treatments in NH — HB 1734 & HB 1735