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TEPID 574665A T (19) (11) EP 2 574 665 A1 EUROPEAN PATENT APPLICATION (12) (43) Date of publication: (51) Int Cl.: C12N 5/07 (2010.01) A61Q 19/00 (2006.01) 03.04.2013 Bulletin 2013/14 G01N 33/50 (2006.01)
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What is procurement isolation and cryopreservation?
Procurement isolation and cryopreservation is a process in which biological materials, such as tissues or organs, are obtained and stored in a controlled environment to maintain their viability and usefulness for future transplantation or research purposes.
Who is required to file procurement isolation and cryopreservation?
The individuals or organizations involved in the procurement and isolation of biological materials are generally required to file documentation related to procurement isolation and cryopreservation. This may include medical providers, research institutions, or transplantation centers, depending on the specific regulations and guidelines of the jurisdiction.
How to fill out procurement isolation and cryopreservation?
To fill out the documentation for procurement isolation and cryopreservation, you will typically need to provide detailed information about the biological materials being procured and isolated, the methods used for isolation and cryopreservation, any relevant donor and recipient information, and any associated ethical considerations. The specific format and requirements may vary depending on the jurisdiction and applicable regulations.
What is the purpose of procurement isolation and cryopreservation?
The purpose of procurement isolation and cryopreservation is to ensure the viability and long-term preservation of biological materials for future use in transplantation, research, or medical advancements. It allows for the availability of these materials when needed, potentially saving lives, advancing scientific knowledge, and improving medical treatments and outcomes.
What information must be reported on procurement isolation and cryopreservation?
The specific information that must be reported on procurement isolation and cryopreservation can vary depending on the jurisdiction and applicable regulations. Generally, it may include details about the biological materials being procured and isolated, the methods used for isolation and cryopreservation, any donor and recipient information, ethical considerations, and any other relevant information required by local authorities or governing bodies.
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