The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jun. 25, 2019

Filed:

Mar. 14, 2014
Applicant:

Lantheus Medical Imaging, Inc., North Billerica, MA (US);

Inventors:

Derek F. Rhodes, North Andover, MA (US);

Robert W. Siegler, Chelmsford, MA (US);

Assignee:

Lantheus Medical Imaging, Inc., North Billerica, MA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G06Q 50/22 (2018.01); G05D 21/02 (2006.01); G06Q 10/06 (2012.01); G06Q 30/00 (2012.01); G05B 15/02 (2006.01);
U.S. Cl.
CPC ...
G05D 21/02 (2013.01); G05B 15/02 (2013.01); G06Q 10/06 (2013.01); G06Q 30/018 (2013.01); G06Q 50/22 (2013.01);
Abstract

Techniques for monitoring a pharmaceutical manufacturing process and making determinations regarding the release of radiopharmaceuticals to health care providers. A data processing system collects data across multiple batches of radiopharmaceuticals, across multiple entities, and/or across multiple stages of the manufacturing process, processes the data, and provides feedback to entities involved in the manufacturing process. In scenarios where quality assurance tests are conducted, data is collected from radiopharmaceutical products before they are shipped, and the data is analyzed to provide the recipients with an indication of whether the radiopharmaceutical products satisfy quality assurance standards. Techniques for analyzing information about a batch manufacturing process and, when a problem occurred during a manufacture of a batch, determining whether to continue to manufacture a next batch in time for delivering and administering to a patient. The detected problem may be investigated and remedied before or during the synthesis of the next batch.


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