
Bringing new innovative inhalation therapies to market is a long and risky process. The interaction of drug and device involves a high degree of complexity where both technical and regulatory requirements must be met. Having this in mind, choosing the ideal nebulizer and device partner can make all the difference and reduce overall development risks.
Rely on PARI as a trusted partner for the most suitable nebulizer - ensuring the best fit to your drug.

March, 2010
Altera® for Cayson®
Approved in US, EU, CAN
July, 2010
eFlow®rapid for ColiFin®
Approved in EU
March, 2015
Tolero® for Vantobra®
Approved in EU

March, 2015
Zirela® for Quinsair™
Approved in CAN, EU
September, 2018
Lamira® for ARIKAYCE®
Approved in US
October, 2020
Lamira® for ARIKAYCE®
Approved in EU
March, 2021
Lamira® for ARIKAYCE®
Approved in JPN
October, 2022
Tolero® for Vantobra®
Approved in CH
Investor (during ATS 2024 podium discussion)
CEO (during ERS 2024)
Learn what made Avalyn Pharma decide to go with a customized eFlow Technology nebulizer. Spoiler: ~8.5 min per dose with an eFlow Open System nebulizer vs ~27 DPI inhalations or 45–60 min on general-purpose nebulizers.

ARIKAYCE® (Phase III label extension)
Mycobacterium avium complex (MAC) Lung disease

L-CsA-I
Bronchiolitis Obliterans Syndrome (BOS) in Lung Transplantation

Inhaled CMS
Non-CF Bronchiectasis

Molgramostim
Autoimmune Pulmonary Alveolar Proteinosis (aPAP)

ARINA-1
Bronchiolitis Obliterans Syndrome (BOS) in Lung Transplantation

ARINA-1
Non-CF Bronchiectasis

AP01
Progressive Pulmonary Fibrosis (PPF)

AP02
Idiopathic Pulmonary Fibrosis (IPF)

RCT1100
Primary Ciliary Dyskinesia (PCD)



Discover how PARI supports you in achieving impactful clinical results and commercial success