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Patient Stories

Patient Advocacy Organizations


Alpha-1 Foundation

The Alpha-1 Foundation is dedicated to providing the leadership and resources that will result in increased research, improved health, worldwide detection and a cure for alpha-1 antitrypsin deficiency.

American Association of Respiratory Care

The AARC is a professional membership association for respiratory care professionals and allied health specialists interested in cardiopulmonary care.

Caring Voice Coalition

Caring Voice Coalition empowers patients living with a life-threatening chronic disease through comprehensive outreach programs and services aimed at financial, emotional and educational support.

Coalition for Hemophilia B

Founded in 1990 by Joyce and John Taylor, a couple whose son was diagnosed with moderate to severe Hemophilia B. The coalition provides patients and their families with information about treatments that will improve quality of life and also works to define new treatment modalities and support efforts to eliminate the disease.

COPD Foundation

The COPD Foundation was established to improve the lives of individuals affected by COPD. The organization focuses on achieving these results through research, education and advocacy programs that will lead to prevention, and someday, a cure for this disease.

GBS/CIDP Foundation International

The Foundation supports patients and families affected by Guillain-Barré syndrome, chronic inflammatory demyelinating polyneuropathy (CIDP) or any of the variants.

Hemophilia Federation of America

This community-based organization serves people with bleeding disorders and their families in the U.S. by strengthening community support and awareness, developing effective local organizations and implementing valuable community-based programs.

Immune Deficiency Foundation

IDF provides accurate and timely information to patients diagnosed with a primary immunodeficiency disease in the U.S.

International Patient Organization for Primary Immunodeficiencies

This association of national patient organizations is dedicated to improving awareness, and access to early diagnosis and optimal treatments for primary immunodeficiency patients worldwide.

Jeffrey Modell Foundation

This global nonprofit organization is dedicated to early diagnoses, treatments and cures for primary immunodeficiency conditions through research, education, public awareness, advocacy, patient support and newborn screening.

National Blood Clot Alliance

The NCBA is a non-profit, voluntary health organization dedicated to advancing the prevention, early diagnosis and successful treatment of life-threatening blood clots such as deep vein thrombosis, pulmonary embolism and clot-provoked stroke.

National Hemophilia Foundation

The NHF is dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders through education, advocacy and research.

National Organization for Rare Diseases

NORD is committed to the identification, treatment and cure of rare disorders through programs of education, advocacy, research and service.

The Foundation for Peripheral Neuropathy

The Foundation helps patients with peripheral neuropathy and their families by providing public awareness, patient support, education and advocacy.

Patient Services, Inc.

PSI focuses on providing support to patients with chronic illnesses who were struggling to keep up with expensive premiums and co-payments.

Plasma Protein Therapeutics Association

PPTA is a trade association representing a unique sector of the biologics and biotechnology industry.

Platelet Disorder Support Association

This non-profit corporation was founded in 1998 to provide information, offer support and encourage research about ITP and other platelet disorders.

World Federation of Hemophilia

WFH provides global leadership to improve and sustain care for people with inherited bleeding disorders, including hemophilia, von Willebrand disease, rare factor deficiencies and inherited platelet disorders.

Safety and Quality in Manufacturing Partners and Organizations


U.S. Food and Drug Administration

The FDA's organization consists of the Office of the Commissioner and four directorates overseeing the core functions of the agency: Medical Products and Tobacco, Foods and Veterinary Medicine, Global Regulatory Operations and Policy, and Operations. The FDA licenses and inspects all plasma donation centers.

Clinical Laboratory Improvement Amendments

CLIA regulates laboratory testing and requires clinical labs and and require clinical laboratories to be certificated by their state as well as the Center for Medicare and Medicaid Services (CMS) before they can accept human samples for diagnostic testing. All Grifols plasma donor centers must meet CLIA regulations.

COLA

COLA is a physician-directed organization that promotes excellence in laboratory medicine and patient care through a program of voluntary education, consultation and accreditation.

European Medicines Agency

The EMA is a decentralized agency responsible for the scientific evaluation of medicines developed by pharmaceutical companies for use in the European Union. EMA inspects and licenses many Grifols plasma donor centers.

Current Good Manufacturing Practices

Current Good Manufacturing Practices (cGMP) are followed by pharmaceutical and biotech firms to ensure the products they make meet specific requirements for identity, strength, quality and purity.

International Quality Plasma Program

IQPP provides independent, third-party evaluation and recognition of a plasma donation center's adherence to global industry standards for source plasma.

Regierungspräsidium Darmstadt (Regional Council Darmstadt)

RPDA is the German Health Authority that inspects and licenses many Grifols plasma donation centers.