Pulmonary Fibrosis Foundation

Pulmonary Fibrosis Foundation

Non Profit Organization Management, 811 W Evergreen Ave Ste 204, Chicago, Illinois, 60642, United States, 11-50 Employees

pulmonaryfibrosis.org

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Who is PULMONARY FIBROSIS FOUNDATION

We imagine a world without pulmonary fibrosis. The Pulmonary Fibrosis Foundation is focused on our mission to act as the trusted resource for all who are affected by this disease. Our sig...

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  • 811 W Evergreen Ave Ste 204, Chicago, Illinois, 60642, United States Headquarters: 811 W Evergreen Ave Ste 204, Chicago, Illinois, 60642, United States
  • 11-50 Employees: 11-50
  • dollar-icon Revenue: $1 Million to $5 Million

industries-icon Industry: Non Profit Organization Management

SIC SIC Code: 7389 | NAICS Code: 621999 | Show More

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Pulmonary Fibrosis Foundation Org Chart and Mapping

Employees

Zoe Bubany

Vice President, Board and External Relations

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Frequently Asked Questions Regarding Pulmonary Fibrosis Foundation

Answer: Pulmonary Fibrosis Foundation's headquarters are located at 811 W Evergreen Ave Ste 204, Chicago, Illinois, 60642, United States

Answer: Pulmonary Fibrosis Foundation's phone number is +18*********

Answer: Pulmonary Fibrosis Foundation's official website is https://pulmonaryfibrosis.org

Answer: Pulmonary Fibrosis Foundation's revenue is $1 Million to $5 Million

Answer: Pulmonary Fibrosis Foundation's SIC: 7389

Answer: Pulmonary Fibrosis Foundation's NAICS: 621999

Answer: Pulmonary Fibrosis Foundation has 11-50 employees

Answer: Pulmonary Fibrosis Foundation is in Non Profit Organization Management

Answer: Pulmonary Fibrosis Foundation contact info: Phone number: +18********* Website: https://pulmonaryfibrosis.org

Answer: We imagine a world without pulmonary fibrosis. The Pulmonary Fibrosis Foundation is focused on our mission to act as the trusted resource for all who are affected by this disease. Our signature programs include: PFF Care Center Network PFF Patient Registry PFF Patient Communication Center PFF Ambassador Program An international network of support groups and online communities The PFF Summit Comprehensive disease education materials Our expert Medical Advisory Board and the biennial PFF Summit allow us to maintain an ongoing dialogue with physicians, researchers, industry representatives, and the patient community. This creates a collaborative environment that will help us achieve many of our goals. Our peer-reviewed research program supports projects that improve understanding of pulmonary fibrosis and will lead to successful therapies. We have developed significant relationships with industry partners and upheld our position as the honest broker to inform those affected by pulmonary fibrosis of important scientific breakthroughs.

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