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PARI Pharma

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uuid0008l1f

Namestring
PARI Pharma
Legal namestring
PARI GmbH
Websiteurl
paripharma.com
Company typeenum
Private
Founded yearint
1997
Descriptiontext

PARI Pharma (legally PARI GmbH) is a privately-held German pharmaceutical technology company founded in 1997, headquartered near Munich (Starnberg), specializing in aerosol delivery devices and comprehensive inhalation drug development. The company operates as a B2B technology partner rather than a drug developer, providing customized nebulizer platforms that pharmaceutical companies integrate with their inhaled drug formulations across clinical development, regulatory submission, and commercial phases.

PARI's core product is the eFlow Technology platform — a proprietary vibrating mesh nebulizer system that generates precisely defined aerosol particles for targeted lung deposition. The platform differentiates on delivery efficiency (~8.5 minutes per dose versus 45-60 minutes on general-purpose nebulizers) and silent operation. It supports biologics (40% of pipeline), nucleotides (20%), and small molecules (40%), with at least three productized variants: eFlow Technology (the platform), eFlow Open System Nebulizer (customized per drug formulation), and Lamira Nebulizer System (the commercial product delivering Insmed's ARIKAYCE). Manufacturing is conducted at two PARI GMP-qualified sites for both clinical and commercial supply. The portfolio includes 20+ undisclosed projects plus disclosed partnerships with Insmed, Savara, Zambon, Avalyn Pharma, Renovion, and ReCode Therapeutics spanning Phase I through NDA-stage development.

The business model is OEM-embedded B2B device supply and customization. PARI generates revenue by manufacturing and supplying customized eFlow nebulizer systems to pharmaceutical partners, supporting them through device customization, regulatory, and usability stages in exchange for device supply agreements. Pricing is not publicly disclosed. The company has no direct consumer product; its economic exposure is fully tethered to the commercial success and lifecycle of its pharmaceutical partners' drug-device combination products. Notable validated commercial traction exists via ARIKAYCE (Insmed, $433.8M drug revenue in 2025), and an NDA-stage asset (Savara's MOLBREEVI, PDUFA November 2026) is approaching potential conversion.

Short descriptiontext

PARI Pharma (PARI GmbH) is a German pharmaceutical technology partner that develops and manufactures customized eFlow mesh nebulizer systems for pharmaceutical companies' inhaled drug formulations, serving biologic, nucleotide, and small molecule drug developers across clinical and commercial stages.

Operating statusenum
Operating
Ownership categoryenum
akta.pro rankint
HeadquartersStarnberg, Germany
HQ citystring
Starnberg
HQ countrystring
Germany
HQ regionstring
Europe
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
mesh nebulizer technology, inhalation drug delivery, aerosol delivery devices, pharmaceutical device partnering, nebulizer platform customization
Industry1 code
PRIMARYHLAHAIAJ
Nebulizers & Aerosol Drug Delivery Systems
Healthcare & Life Sciences/Medical Devices & Diagnostics/Drug Delivery Devices (Injectors, Pumps, Inhalers)
NAICS code1 code
  • Medical Equipment and Supplies Manufacturing3391
SIC code1 code
  • Surgical & Medical Instruments & Apparatus3841
Product category
Inhalation Drug Delivery Devices
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Nebulizer Device Supply
TypeHardware Sales
Description

PARI supplies customized eFlow nebulizer systems to pharmaceutical partners for clinical and commercial use. Revenue likely derives from device manufacturing, customization services, and ongoing supply agreements with pharmaceutical partners developing inhaled therapies.

pari.com
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Operations, Technology or R&D, Personnel, Supply Chain, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

PARI Pharma develops and supplies customized eFlow mesh nebulizer systems to pharmaceutical companies for the delivery of inhaled therapies. The company operates as a B2B technology partner, providing device development, regulatory support, and commercial-scale manufacturing across biologics, nucleotides, and small molecule drug programs. Their eFlow vibrating membrane platform enables targeted aerosol delivery to the lungs with reduced treatment times relative to conventional nebulizers.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • ~8.5 minutes per dose with eFlow Open System nebulizer vs ~27 DPI inhalations or 45-60 minutes on general-purpose nebulizers
Product overview1 text field

PARI Pharma operates as a specialized nebulizer technology partner for pharmaceutical companies, offering its eFlow Technology platform as the core product for inhalation drug delivery. The portfolio includes the eFlow mesh nebulizer technology (a vibrating membrane-based aerosol delivery system), the eFlow Open System nebulizer for customized drug formulations, and the Lamira Nebulizer System used in commercial products. PARI's platform serves pharmaceutical partners across multiple therapeutic areas including pulmonology, transplant medicine, and rare diseases, with over 20 undisclosed projects in pre-clinical and clinical development spanning biologics (40%), small molecules (40%), and nucleotides (20%).

Product and service3 records
1eFlow Technology
CategoryNebulizer Platform
Description

PARI's proprietary high-end mesh nebulizer technology platform for inhalation drug delivery, featuring vibrating membrane technology that produces a precisely defined aerosol cloud with efficient lung deposition. Customized per partner drug formulation for clinical and commercial supply.

2eFlow Open System Nebulizer
CategoryCustomized Nebulizer Device
Description

A customized version of the eFlow mesh nebulizer designed for specific drug formulations, offering approximately 8.5 minutes per dose delivery time compared to 45-60 minutes with general-purpose nebulizers.

3Lamira Nebulizer System
CategoryCommercial Nebulizer System
Description

PARI's eFlow-based nebulizer system used commercially to deliver ARIKAYCE (amikacin liposome inhalation suspension) for treatment of Mycobacterium avium complex (MAC) lung disease.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierCoreTypeTechnology or Integration
Description

Insmed uses PARI's Lamira Nebulizer System to deliver ARIKAYCE® (Amikacin Liposome Inhalation Suspension) for MAC Lung disease. This is a Phase III label extension partnership. Insmed generates significant revenue ($433.8M in 2025) from ARIKAYCE, demonstrating commercial success of the PARI-delivered product. PARI also mentioned in Insmed's ASPEN trial presentations.

Strategic tierCoreTypeTechnology or Integration
Description

Savara is developing MOLBREEVI (molgramostim) delivered via PARI's eFlow Nebulizer System for autoimmune Pulmonary Alveolar Proteinosis (aPAP). The product is at NDA stage with FDA PDUFA date of November 22, 2026. Patent protection secured in Europe (Patent No. 4121000) and Australia through March 2041. Potential first and only approved therapy for this rare lung disease.

Strategic tierMajorTypeTechnology or Integration
Description

Zambon is developing L-CsA-I (Inhaled Cyclosporine) for Bronchiolitis Obliterans Syndrome (BOS) in Lung Transplantation and Inhaled CMS for Non-CF Bronchiectasis, both using PARI's eFlow Technology. Both programs are in Phase III development.

Strategic tierMajorTypeTechnology or Integration
Description

Avalyn Pharma uses customized eFlow Technology nebulizers for AP01 (inhaled pirfenidone) targeting Progressive Pulmonary Fibrosis. The Phase 2b MIST trial enrolled 375 patients with topline results expected in H2 2027. Avalyn also developing AP02 for Idiopathic Pulmonary Fibrosis using the same platform.

Strategic tierSupportingTypeTechnology or Integration
Description

Renovion is developing ARINA-1 for respiratory conditions using PARI's eFlow Technology at Phase II stage.

Strategic tierSupportingTypeTechnology or Integration
Description

ReCode Therapeutics is developing RCT1100 for Primary Ciliary Dyskinesia (PCD) using PARI's eFlow Technology at Phase I stage.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Nemera is a drug delivery device company with a dedicated inhalation franchise including nebulizer and related respiratory devices. It serves pharmaceutical partners developing inhaled therapies with custom device solutions, comparable to PARI's OEM-embedded model.

TypeOthers
Description

Copley Scientific supplies testing equipment and services for inhaler and nebulizer development, including cascade impactors and aerodynamic particle sizing. It serves the same pharmaceutical R&D ecosystem that PARI addresses as an enabling equipment vendor.

TypeDirect peer
Description

Kindeva (formerly 3M Drug Delivery Systems) is a leading CDMO offering formulation and device development services for inhaled pharmaceuticals, including nebulizer, DPI, and pMDI programs. It competes with PARI on partner selection for inhaled drug development projects.

TypeDirect peer
Description

Aerogen is the leading vibrating mesh nebulizer manufacturer focused on hospital and acute care aerosol drug delivery. It competes most directly with PARI's eFlow platform in the high-performance mesh nebulizer category serving pharmaceutical partners and clinical applications.

TypeDirect peer
Description

Owen Mumford is a drug delivery device manufacturer with capabilities spanning injectors, inhalation, and other delivery routes. It provides custom device development services to pharmaceutical partners in adjacent drug delivery categories to PARI.

TypeBroad incumbent
Description

Catalent is a large pharmaceutical services CDMO with inhalation development and manufacturing capabilities. It competes with PARI in offering integrated inhalation drug product services to pharma partners and serves as an alternative development partner.

TypeDirect peer
Description

Hovione is a contract development and manufacturing organization with strong inhalation drug product capabilities spanning APIs, formulation, and device integration. It offers an alternative integrated platform to pharmaceutical partners developing inhaled therapies.

TypeBroad incumbent
Description

Vectura, acquired by Philip Morris International, is a specialist inhalation drug delivery company with DPI and nebulizer device platforms. It serves comparable pharmaceutical partners across the inhaled therapy development pipeline.

TypeDirect peer
Description

Bespak, now part of Recipharm, is a specialist in inhalation and nasal drug delivery devices including pMDIs and DPIs. It provides device development and commercial supply services to pharmaceutical partners developing inhaled therapeutics.

TypeBroad incumbent
Description

Aptar Pharma is a global leader in drug delivery devices across nasal, pulmonary, ophthalmic, and injectable modalities. It competes broadly in inhalation device development and supply as part of a wider drug delivery portfolio.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers6 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

PARI Pharma

Inhalation Drug Delivery Devicesparipharma.com

PARI Pharma (PARI GmbH) is a German pharmaceutical technology partner that develops and manufactures customized eFlow mesh nebulizer systems for pharmaceutical companies' inhaled drug formulations, serving biologic, nucleotide, and small molecule drug developers across clinical and commercial stages.

What PARI Pharma does

PARI Pharma (legally PARI GmbH) is a privately-held German pharmaceutical technology company founded in 1997, headquartered near Munich (Starnberg), specializing in aerosol delivery devices and comprehensive inhalation drug development. The company operates as a B2B technology partner rather than a drug developer, providing customized nebulizer platforms that pharmaceutical companies integrate with their inhaled drug formulations across clinical development, regulatory submission, and commercial phases.

PARI's core product is the eFlow Technology platform — a proprietary vibrating mesh nebulizer system that generates precisely defined aerosol particles for targeted lung deposition. The platform differentiates on delivery efficiency (~8.5 minutes per dose versus 45-60 minutes on general-purpose nebulizers) and silent operation. It supports biologics (40% of pipeline), nucleotides (20%), and small molecules (40%), with at least three productized variants: eFlow Technology (the platform), eFlow Open System Nebulizer (customized per drug formulation), and Lamira Nebulizer System (the commercial product delivering Insmed's ARIKAYCE). Manufacturing is conducted at two PARI GMP-qualified sites for both clinical and commercial supply. The portfolio includes 20+ undisclosed projects plus disclosed partnerships with Insmed, Savara, Zambon, Avalyn Pharma, Renovion, and ReCode Therapeutics spanning Phase I through NDA-stage development.

The business model is OEM-embedded B2B device supply and customization. PARI generates revenue by manufacturing and supplying customized eFlow nebulizer systems to pharmaceutical partners, supporting them through device customization, regulatory, and usability stages in exchange for device supply agreements. Pricing is not publicly disclosed. The company has no direct consumer product; its economic exposure is fully tethered to the commercial success and lifecycle of its pharmaceutical partners' drug-device combination products. Notable validated commercial traction exists via ARIKAYCE (Insmed, $433.8M drug revenue in 2025), and an NDA-stage asset (Savara's MOLBREEVI, PDUFA November 2026) is approaching potential conversion.

PARI Pharma firmographics

Firmographics
Name
PARI Pharma
Legal name
PARI GmbH
Website
https://paripharma.com
Company type
Private
Founded year
1997
Operating status
Operating
Short description
PARI Pharma (PARI GmbH) is a German pharmaceutical technology partner that develops and manufactures customized eFlow mesh nebulizer systems for pharmaceutical companies' inhaled drug formulations, serving biologic, nucleotide, and small molecule drug developers across clinical and commercial stages.
Ownership category
akta.pro rank

PARI Pharma industry classification

Industry
Product category
Inhalation Drug Delivery Devices
NAICS
Medical Equipment and Supplies Manufacturing (3391)
SIC
Surgical & Medical Instruments & Apparatus (3841)
akta.pro industry
PRIMARYHLAHAIAJ
Nebulizers & Aerosol Drug Delivery Systems
Healthcare & Life Sciences/Medical Devices & Diagnostics/Drug Delivery Devices (Injectors, Pumps, Inhalers)

Keywords

  • Mesh nebulizer technology
  • Inhalation drug delivery
  • Aerosol delivery devices
  • Pharmaceutical device partnering
  • Nebulizer platform customization

Where PARI Pharma is headquartered

Location

Headquarters

HQ city
Starnberg
HQ country
Germany
HQ region
Europe

Offices1 record

Markets served

PARI Pharma business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Operations, Technology or R&D, Personnel, Supply Chain, Marketing or Sales

Revenue model

  1. Nebulizer Device Supply: PARI supplies customized eFlow nebulizer systems to pharmaceutical partners for clinical and commercial use. Revenue likely derives from device manufacturing, customization services, and ongoing supply agreements with pharmaceutical partners developing inhaled therapies.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels3 records

PARI Pharma product offering

Product offering

Core offering

PARI Pharma develops and supplies customized eFlow mesh nebulizer systems to pharmaceutical companies for the delivery of inhaled therapies. The company operates as a B2B technology partner, providing device development, regulatory support, and commercial-scale manufacturing across biologics, nucleotides, and small molecule drug programs. Their eFlow vibrating membrane platform enables targeted aerosol delivery to the lungs with reduced treatment times relative to conventional nebulizers.

Product overview

PARI Pharma operates as a specialized nebulizer technology partner for pharmaceutical companies, offering its eFlow Technology platform as the core product for inhalation drug delivery. The portfolio includes the eFlow mesh nebulizer technology (a vibrating membrane-based aerosol delivery system), the eFlow Open System nebulizer for customized drug formulations, and the Lamira Nebulizer System used in commercial products. PARI's platform serves pharmaceutical partners across multiple therapeutic areas including pulmonology, transplant medicine, and rare diseases, with over 20 undisclosed projects in pre-clinical and clinical development spanning biologics (40%), small molecules (40%), and nucleotides (20%).

Differentiator

Problem solved

Functional benefit

Products and services

  • eFlow Technology PARI's proprietary high-end mesh nebulizer technology platform for inhalation drug delivery, featuring vibrating membrane technology that produces a precisely defined aerosol cloud with efficient lung deposition. Customized per partner drug formulation for clinical and commercial supply.
  • eFlow Open System Nebulizer A customized version of the eFlow mesh nebulizer designed for specific drug formulations, offering approximately 8.5 minutes per dose delivery time compared to 45-60 minutes with general-purpose nebulizers.
  • Lamira Nebulizer System PARI's eFlow-based nebulizer system used commercially to deliver ARIKAYCE (amikacin liposome inhalation suspension) for treatment of Mycobacterium avium complex (MAC) lung disease.

Quantifiable outcome

  • ~8.5 minutes per dose with eFlow Open System nebulizer vs ~27 DPI inhalations or 45-60 minutes on general-purpose nebulizers

Companies that use PARI Pharma

Customer profile

Named customers6 records

Segments3 records

Ideal customer profiles1 record

PARI Pharma technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

PARI Pharma partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered core, major and supporting.

  • Insmed IncorporatedcoreTechnology or IntegrationInsmed uses PARI's Lamira Nebulizer System to deliver ARIKAYCE® (Amikacin Liposome Inhalation Suspension) for MAC Lung disease. This is a Phase III label extension partnership. Insmed generates significant revenue ($433.8M in 2025) from ARIKAYCE, demonstrating commercial success of the PARI-delivered product. PARI also mentioned in Insmed's ASPEN trial presentations.
  • Savara Inc.coreTechnology or IntegrationSavara is developing MOLBREEVI (molgramostim) delivered via PARI's eFlow Nebulizer System for autoimmune Pulmonary Alveolar Proteinosis (aPAP). The product is at NDA stage with FDA PDUFA date of November 22, 2026. Patent protection secured in Europe (Patent No. 4121000) and Australia through March 2041. Potential first and only approved therapy for this rare lung disease.
  • ZambonmajorTechnology or IntegrationZambon is developing L-CsA-I (Inhaled Cyclosporine) for Bronchiolitis Obliterans Syndrome (BOS) in Lung Transplantation and Inhaled CMS for Non-CF Bronchiectasis, both using PARI's eFlow Technology. Both programs are in Phase III development.
  • Avalyn PharmamajorTechnology or IntegrationAvalyn Pharma uses customized eFlow Technology nebulizers for AP01 (inhaled pirfenidone) targeting Progressive Pulmonary Fibrosis. The Phase 2b MIST trial enrolled 375 patients with topline results expected in H2 2027. Avalyn also developing AP02 for Idiopathic Pulmonary Fibrosis using the same platform.
  • RenovionsupportingTechnology or IntegrationRenovion is developing ARINA-1 for respiratory conditions using PARI's eFlow Technology at Phase II stage.
  • ReCode TherapeuticssupportingTechnology or IntegrationReCode Therapeutics is developing RCT1100 for Primary Ciliary Dyskinesia (PCD) using PARI's eFlow Technology at Phase I stage.

Scale indicators3 records

Recent moves6 records

Expansion highlights5 records

PARI Pharma competitors and assessment

Company assessment

Direct peers

  • Nemera: Nemera is a drug delivery device company with a dedicated inhalation franchise including nebulizer and related respiratory devices. It serves pharmaceutical partners developing inhaled therapies with custom device solutions, comparable to PARI's OEM-embedded model.
  • Kindeva Drug Delivery: Kindeva (formerly 3M Drug Delivery Systems) is a leading CDMO offering formulation and device development services for inhaled pharmaceuticals, including nebulizer, DPI, and pMDI programs. It competes with PARI on partner selection for inhaled drug development projects.
  • Aerogen: Aerogen is the leading vibrating mesh nebulizer manufacturer focused on hospital and acute care aerosol drug delivery. It competes most directly with PARI's eFlow platform in the high-performance mesh nebulizer category serving pharmaceutical partners and clinical applications.
  • Owen Mumford: Owen Mumford is a drug delivery device manufacturer with capabilities spanning injectors, inhalation, and other delivery routes. It provides custom device development services to pharmaceutical partners in adjacent drug delivery categories to PARI.
  • Hovione: Hovione is a contract development and manufacturing organization with strong inhalation drug product capabilities spanning APIs, formulation, and device integration. It offers an alternative integrated platform to pharmaceutical partners developing inhaled therapies.
  • Bespak (Recipharm): Bespak, now part of Recipharm, is a specialist in inhalation and nasal drug delivery devices including pMDIs and DPIs. It provides device development and commercial supply services to pharmaceutical partners developing inhaled therapeutics.

Others

  • Copley Scientific: Copley Scientific supplies testing equipment and services for inhaler and nebulizer development, including cascade impactors and aerodynamic particle sizing. It serves the same pharmaceutical R&D ecosystem that PARI addresses as an enabling equipment vendor.

Broad incumbents

  • Catalent (Novo Holdings): Catalent is a large pharmaceutical services CDMO with inhalation development and manufacturing capabilities. It competes with PARI in offering integrated inhalation drug product services to pharma partners and serves as an alternative development partner.
  • Vectura (Philip Morris): Vectura, acquired by Philip Morris International, is a specialist inhalation drug delivery company with DPI and nebulizer device platforms. It serves comparable pharmaceutical partners across the inhaled therapy development pipeline.
  • Aptar Pharma: Aptar Pharma is a global leader in drug delivery devices across nasal, pulmonary, ophthalmic, and injectable modalities. It competes broadly in inhalation device development and supply as part of a wider drug delivery portfolio.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights6 records

Customer concentration

PARI Pharma social profiles

Digital presence

PARI Pharma financial estimates

Financial estimate

Revenue estimate

Valuation estimate

PARI Pharma leadership team

Management profile

Number of profiles

PARI Pharma funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

PARI Pharma M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about PARI Pharma

What does PARI Pharma do?

PARI Pharma develops and supplies customized eFlow mesh nebulizer systems to pharmaceutical companies for the delivery of inhaled therapies. The company operates as a B2B technology partner, providing device development, regulatory support, and commercial-scale manufacturing across biologics, nucleotides, and small molecule drug programs. Their eFlow vibrating membrane platform enables targeted aerosol delivery to the lungs with reduced treatment times relative to conventional nebulizers.

Is PARI Pharma a public or private company?

PARI Pharma is a private company. It is classified as unknown and is currently operating.

When was PARI Pharma founded?

PARI Pharma was founded in 1997.

Where is PARI Pharma based?

PARI Pharma is headquartered in Starnberg, Germany, in the Europe region.

How does PARI Pharma make money?

One revenue line is on record: nebulizer Device Supply.

Who are PARI Pharma's main competitors?

Direct peers on record are Nemera, Kindeva Drug Delivery, Aerogen, Owen Mumford, Hovione and Bespak (Recipharm). Copley Scientific is listed as an others. Broad incumbents are Catalent (Novo Holdings), Vectura (Philip Morris) and Aptar Pharma.

Does PARI Pharma have an API?

No public API is recorded for PARI Pharma.

What industry is PARI Pharma in?

PARI Pharma's product category is Inhalation Drug Delivery Devices. Its primary akta.pro industry code is HLAHAIAJ, Nebulizers & Aerosol Drug Delivery Systems. Its NAICS code is 3391 and its SIC code is 3841.

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Live signals
PR NewswireDr. Stefan Seemann is appointed President of PARI Pharma GmbHDr. Stefan Seemann has been appointed President of PARI Pharma GmbH, succeeding Dr. Martin Knoch who is retiring after over 30 years with the company. The leadership transition, effective July 1, 2021, aims to ensure continuity in PARI's development of eFlow Technology and its position as a market leader in cystic fibrosis therapies.PR NewswireWorldwide Portable Compressor Nebulizer Industry to 2025 - Increasing Demand for Home Healthcare Devices Presents OpportunitiesResearch and Markets has released a global market research report projecting the portable compressor nebulizer market to grow from USD 317.25 million in 2020 to USD 476.16 million by 2025, representing an 8.46% CAGR, driven by rising incidences of chronic respiratory diseases and increasing demand for home healthcare devices. The report provides segmentation by type, application, distribution channel, and geography, with North America projected to lead the market. Recent developments include Koninklijke Philips launching the InnoSpire Go portable nebulizer in November 2018 and Pari Pharma receiving approval for its LAMIRA e-FLOW technology device in October 2018.PR NewswireLAMIRA®, an eFlow® Technology nebulizer, expected to launch in Japan as a medical device for exclusive administration of ARIKAYCE® (amikacin liposome inhalation suspension)PARI Pharma GmbH announced the authorization of the LAMIRA Nebulizer System for delivery of Insmed's drug product ARIKAYCE in Japan, following MHLW approval on March 23, 2021. LAMIRA is the first drug-specific eFlow Technology nebulizer registered beyond Europe and North America, and ARIKAYCE is the first and only therapy in Japan indicated for patients with nontuberculous mycobacterial lung disease caused by MAC who did not respond to prior treatment. The launch marks an expansion of the PARI-Insmed partnership into a new geographic market, offering a new treatment option for patients with refractory NTM lung disease in Japan.PR NewswireARIKAYCE® (amikacin liposome inhalation suspension) Approved by Japan's Ministry of Health, Labour and Welfare for the Treatment of Patients with NTM Lung Disease Caused by MAC Who Did Not SufficientlJapan's Ministry of Health, Labour and Welfare approved Insmed Incorporated's ARIKAYCE (amikacin liposome inhalation suspension) for treating patients with nontuberculous mycobacterial lung disease caused by MAC who did not respond to prior multidrug therapy. The approval was based on the Phase 3 CONVERT study, which demonstrated improved sputum culture conversion rates with ARIKAYCE combined with background multidrug regimen compared to background therapy alone. The company anticipates launching ARIKAYCE in Japan in mid-2021, marking its third major regulatory approval following US and European authorizations.PR NewswireInsmed Reports First Quarter 2019 Financial Results and Provides Business UpdateInsmed Incorporated reported first quarter 2019 financial results with total revenue of $21.9 million and a net loss of $74.2 million, compared to a net loss of $68.5 million in Q1 2018. The company provided an update on the U.S. launch of ARIKAYCE, the first and only FDA-approved treatment for refractory MAC lung disease, reporting steady increases in new patients and prescribers along with strong payer trends. Insmed also announced progress on global expansion to Europe and Japan, completion of enrollment for the WILLOW study of INS1007, and full-year 2019 revenue guidance of $90-105 million for ARIKAYCE.PR NewswirePARI Pharma's eFlow® Technology device, LAMIRA™, approved as the only nebulizer system to deliver Insmed's ARIKAYCE® (amikacin liposome inhalation suspension)PARI Pharma GmbH's LAMIRA nebulizer system received FDA accelerated approval on September 28, 2018, as the delivery device for Insmed Incorporated's ARIKAYCE (amikacin liposome inhalation suspension), making it the first and only FDA-approved therapy for Mycobacterium avium complex (MAC) lung disease. ARIKAYCE represents a novel inhaled formulation of amikacin that uses Insmed's Pulmovance liposomal technology to deliver the antibiotic directly to the lungs, targeting lung macrophages where the infection resides while limiting systemic toxicity. LAMIRA is the third FDA approval where PARI Pharma's eFlow Technology vibrating membrane nebulizer was used exclusively to deliver an approved drug, developed through close collaboration between PARI Pharma and Insmed.PR NewswirePneumatic Nebulizers Market is expected to expected to reach a value of USD 893.9 million by 2025The global pneumatic nebulizers market was valued at USD 490.6 million in 2015 and is projected to reach USD 893.9 million by 2025, driven by an aging population, growing demand for home healthcare portable devices, and new aerosol drug delivery technologies that minimize drug wastage. Several companies have taken strategic actions to capitalize on this growth, including Philips receiving FDA 510(k) clearance for its cloud-based Care Orchestrator platform in March 2016 and Sunovion Pharmaceuticals initiating Phase III clinical trials using PARI Pharma's eFlow nebulizer system in March 2015. The Asia Pacific region is identified as the fastest-growing market due to its large aging population, increasing focus on preventive care, and government initiatives promoting technological innovation.PR NewswireEntwicklung von PARI Pharma mit eFlow Technologie gegen Bronchiolitis Obliterans Syndrom (BOS) wird an Breath Therapeutics lizenziertPARI Pharma has licensed its first-in-class Bronchiolitis Obliterans Syndrome (BOS) inhalation development program to Breath Therapeutics GmbH, making it Breath Therapeutics' lead program. Breath Therapeutics recently closed a €43.5 million Series A financing round to advance the program into Phase III clinical trials in Europe and the United States. PARI Pharma had previously completed Phase I and II trials confirming the safety and clinical efficacy of liposomal Cyclosporin A formulated for its eFlow technology platform.PR NewswirePARI Pharma development featuring eFlow Technology for Bronchiolitis Obliterans Syndrome (BOS) is licensed to Breath TherapeuticsPARI Pharma has licensed its first-in-class inhalation development program for Bronchiolitis Obliterans Syndrome (BOS) to Breath Therapeutics GmbH as their lead program. Breath Therapeutics recently closed on 43.5 million Euros in Series A financing to fund the advancement of the program into Phase III clinical trials in Europe and the US. The development combines PARI's proprietary liposomal cyclosporine A formulation with its eFlow Technology device platform, which includes remote adherence monitoring features.PR NewswirePARI Pharma's Investigational Closed eFlow Nebulizer System Used in Two Successful Phase 3 Clinical Studies Evaluating Sunovion's SUN-101 (glycopyrrolate) in People with Moderate-to-Very Severe ChroniPARI Pharma announced that its investigational closed eFlow nebulizer system was used in two pivotal Phase 3 clinical trials for Sunovion's SUN-101 (glycopyrrolate), a long-acting muscarinic antagonist for moderate-to-very severe COPD. The trials met their primary endpoint, showing statistically significant improvement in trough FEV1 at week 12 for both the 25 mcg and 50 mcg twice-daily dose groups versus placebo. The closed eFlow device is designed to deliver medication in two to three minutes compared to standard jet nebulizers that typically take up to 10 minutes.