Beth Keyt
Conseiller Juridique Général chez PEAR THERAPEUTICS, INC.
Profil
Beth Keyt is currently the Vice President of Government Affairs and Market Access at Pear Therapeutics, Inc. She previously worked as the Senior Director of US Government at DexCom, Inc. Ms. Keyt received an undergraduate degree from the University of Connecticut.
Postes actifs de Beth Keyt
| Sociétés | Poste | Début |
|---|---|---|
| PEAR THERAPEUTICS, INC. | Conseiller Juridique Général | - |
Anciens postes connus de Beth Keyt
| Sociétés | Poste | Fin |
|---|---|---|
| DEXCOM, INC. | Corporate Officer/Principal | - |
Formation de Beth Keyt
| University of Connecticut | Undergraduate Degree |
Expériences
Fonctions occupées
Relations
Relations au 1er degré
Entreprises liées au 1er degré
Homme
Femme
Administrateurs
Exécutifs
Sociétés liées
| Sociétés cotées | 1 |
|---|---|
| DEXCOM, INC. | Health Technology |
| Entreprise privées | 1 |
|---|---|
Pear Therapeutics, Inc.
 Pear Therapeutics, Inc. Medical SpecialtiesHealth Technology Pear Therapeutics, Inc. is a commercial-stage healthcare company pioneering a new class of software-based medicines, sometimes referred to as Prescription Digital Therapeutics (PDT), which use software to treat diseases directly. The firm aims to redefine medicine by discovering, developing, and delivering clinically validated software-based therapeutics to provide better outcomes for patients, smarter engagement and tracking tools for clinicians, and cost-effective solutions for payers. It has a pipeline of products and product candidates across therapeutic areas, including the first three PDTs with disease treatment claims from the FDA. The company’s lead product, reSET, for the treatment of substance use disorder, was the first PDT to receive marketing authorization from the FDA to treat disease. Its second product, reSET-O, for the treatment of opioid use disorder, was the first PDT to receive Breakthrough Designation. Pear's third product, Somryst for the treatment of chronic insomnia, was the first PDT submitted through the FDA's traditional 510(k) pathway while simultaneously reviewed through the FDA's Software Precertification Pilot Program. The company was founded on December 1, 2020 and is headquartered in Boston, MA. | Health Technology |