Our Customization Approach &

How it Supports Your Drug Development Process

Ensuring the best Fusion of Your Formulation with our eFlow^® Technology.

We use our extensive customization options to define the ideal nebulizer for your formulation. This reduces the overall risk and saves you time on the way to a commercial product.

Your drug formulation

Feasibility

In-vitro aerosol performance testing with eFlow^® Technology components to select the best configuration for you.

Development

Device optimization and support of clinical trials

Commercialization

Final regulatory submission, launch preparation and post-launch activities.

Expert Interviews

Get more details from our experts on the evaluation phase and nebulizer customization:

Jonas Knoch, Business Development Manager eFlow, provides valuable insights into the early evaluation of drug formulation and nebulizer.

Dr. Markus Tservistas, Senior Project Leader eFlow, explains how the previous evaluation work is continued in the development stage and how we can support clinical trials and regulatory submissions.

Dr. Benjamin Heine, Technology Platform Leader eFlow, gives you an idea of the methods used to customize eFlow® Technology nebulizers for your drug formulation.

Developing new drug-nebulizer combination products

Learn more about bringing a new a drug-device combination product to the market.

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eFlow® Technology Platform: Offers Proven Flexibility and Performance

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eFlow Open System

Highly efficient nebulizer platform, well-established in several commercial products.

eFlow Integrated

Innovative breath-triggered nebulizer platform with breath-guiding (under development).

Discover more

Laser-Drilled Vibrating Mesh

Our eFlow Technology, refined over 20 years, features a laser-drilled vibrating mesh. Today the platform offers a wide range of validated meshes to optimize aerosol performance and ensure ideal delivery efficiency.

By tailoring aerosol parameters to your specific needs we can improve efficacy of your formulation.

How you benefit

Full support and reliability to keep your program on track through PARI expertise and know-how
Fostering positive results in safety and efficacy studies with reduced nominal doses through high delivery efficiency
Optimized development path through proven modular and flexible device platform that can quickly be adapted to your specific requirements.
In-house services: Aerosol lab (GMP and ISO13485-certified), usability and regulatory expertise – everything goes hand in hand to provide required reports and documentation
Exclusivity agreements: To strengthen your market position

Laser vibrometer to analyze the vibration of the mesh.

Secure your slot for a feasibility assessment in our lab!

eFlow-partneringpari.com

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