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Health Canadas Safety of Human Cells, Tissues and Organs for Transplantation Regulations (or CTO Regulations) is legally binding [29]. The purpose of the CTO Regulations is to minimize the potential health risks to Canadian recipients of human cells, tissues and organs for transplantation.
The CTO Regulations require that source establishment and establishments that distribute or import cells, tissues or organs register with Health Canada. Establishments that only retrieve CTO, only import for transplant, or only transplant do not have to register.
There are only four requirements for a valid adverse drug reaction report: patient identifier, medicine, reaction, reporter details.
The CTO regulations set forth requirements for establishment registration, and processing (which encompasses collection, donor screening, donor testing, assessment of donor suitability, packaging and labeling, and quarantine).
Health Canadas Safety of Human Cells, Tissues and Organs for Transplantation Regulations (or CTO Regulations) is legally binding [29]. The purpose of the CTO Regulations is to minimize the potential health risks to Canadian recipients of human cells, tissues and organs for transplantation.
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When are Adverse Event Reports Required by Health Canada? Death of a patient, user or other person. Serious deterioration in health of a patient, user or other person. Potential for death or serious deterioration in health of a patient, user or other person if the incident were to recur.
Sale of tissue prohibited 10 A person must not buy, sell or otherwise deal in, directly or indirectly, for a valuable consideration, any tissue for a transplant, or any body or parts other than blood or a blood constituent, for therapeutic purposes, medical education or scientific research.

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