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Urgent FIELD SAFETY NOTICE Device: Term Advanced Perfusion System 1: Interface Modules for CDI TM Systems & Serial Data Transfer Reference: Action: FSN1210 2012-12 Field Replacement Attention: Chief
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20 february - swissmedic refers to the deadline for submitting certain regulatory information to the Swiss Agency for Therapeutic Products (Swissmedic) on the 20th of February.
Any company or individual involved in the production, distribution, or sale of pharmaceutical products in Switzerland may be required to file regulatory information on 20 february - swissmedic.
The specific process for filling out 20 february - swissmedic depends on the type of information being submitted. Generally, it involves completing the necessary forms and providing accurate and up-to-date information as required by Swissmedic.
The purpose of 20 february - swissmedic is to ensure compliance with regulatory requirements and to facilitate the monitoring and evaluation of pharmaceutical products in Switzerland. It allows Swissmedic to assess the quality, safety, and efficacy of these products.
The specific information that must be reported on 20 february - swissmedic depends on the regulatory obligations applicable to the company or individual. It may include details about product registrations, clinical trials, adverse events, manufacturing processes, labeling, and other related information.
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