FDA reg­u­la­tions 101: medTech edi­tion — US mar­ket, online

Are you a Finnish MedTech com­pa­ny look­ing to expand into the U.S. mar­ket?

Under­stand­ing the com­plex reg­u­la­to­ry land­scape of the FDA is cru­cial for your suc­cess. Join the expert-led webi­nar organ­ised by Busi­ness Fin­land to gain a com­pre­hen­sive overview of U.S. MedTech reg­u­la­tions, includ­ing device clas­si­fi­ca­tions, 510(k) clear­ance, PMA path­ways, qual­i­ty sys­tem require­ments, and post-mar­ket sur­veil­lance. Learn about the chal­lenges and oppor­tu­ni­ties, and get insights to stream­line your FDA approval process, ensur­ing a smooth entry into the U.S. mar­ket.

Time: 7 Novem­ber 2024 at 16:00–17:00 (Finnish time)

Place: Microsoft Teams Webi­nar

Reg­is­tra­tion

Con­tact per­sons

Tit­ta Houni
Senior Advi­sor, Busi­ness Fin­land
titta.houni (at) businessfinland.fi

Prac­ti­cal­i­ties:
Jeni Sär­mäkari
Pro­gram Coor­di­na­tor
jeni.sarmakari (at) businessfinland.fi

Source: Busi­ness Fin­land