Cardinal Health expands PET nuclear pharmacy services to support clinical drug trials | Nuclear Molecular
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Communities Nuclear/Molecular Cardinal Health expands PET nuclear pharmacy services to support clinical drug trials

Cardinal Health expands PET nuclear pharmacy services to support clinical drug trials

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Cardinal Health, a global provider of healthcare products and services, has announced that it will now manufacture, compound and distribute PET radiopharmaceuticals for clinical trials.

Cardinal Health, a global provider of healthcare products and services, has announced that it will now manufacture, compound and distribute positron emission tomography (PET) radiopharmaceuticals for clinical trials.

The company's new services for the clinical trial market will be discussed at the Society of Nuclear Medicine's (SNM) 55th Annual Meeting, taking place in New Orleans, June 14-18.

Cardinal Health owns and operates a network of more than 150 nuclear pharmacies and operates 25 cyclotron-based PET radiopharmaceutical manufacturing facilities. These facilities are registered with the Food and Drug Administration (FDA) to manufacture PET radiopharmaceuticals that are used by physicians to diagnose various medical conditions.

The company will now offer its PET manufacturing and distribution services to support clinical trials of new and novel PET agents. Cardinal Health will also work with pharmaceutical companies and physicians interested in using PET products to determine the efficacy of therapeutic medications.

"We're committed to advancing the future of molecular imaging by helping manufacturers expand the pipeline of new agents that will aid in the diagnosis and treatment of disease," said John Rademacher, general manager of nuclear pharmacy services for Cardinal Health. "By supporting the clinical trial phase of PET drug development, we will also build strong, long-term partnerships as these products move through the testing and approval phase and into routine clinical application."

Cardinal Health will also submit drug master files to the FDA for several of the PET agents it manufactures. These files contain detailed information about the manufacturing and storing of a specific drug and can help expand the use of PET products because they allow physicians and others in the pharmaceutical industry to test PET agents in the treatment or diagnosis of disease without needing to re-file drug manufacturing information with the FDA.

 

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