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Received by Swiss medic (please leave blank)Form for the approval of Category C trials. Before completing this form, please refer to the information sheet BW510×00_001e×MB_Information×Sheet×Clinical×Trials×MD.document
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01
carefully read the received document from Swissmedic
02
understand the purpose of the form and the information required
03
gather all the necessary information and documents
04
fill out the form accurately and completely
05
double-check the filled form for any errors or omissions
06
ensure all required fields are completed
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provide any supporting documents or attachments as requested
08
review the completed form for accuracy and completeness
09
sign and date the form, if required
10
submit the filled form to Swissmedic as per their instructions

Who needs received by swissmedic please?

01
Any individual, organization, or company who is required to submit regulatory information or seek approval from Swissmedic may need to fill out the received by Swissmedic form.

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Received by Swissmedic refers to any documentation or reports that are submitted to the Swiss Agency for Therapeutic Products.
Any individual or organization involved in the manufacturing, distribution, or marketing of therapeutic products in Switzerland may be required to file received by Swissmedic.
Received by Swissmedic can typically be filled out online through the Swissmedic website or submitted via mail or email following the specific guidelines provided.
The purpose of received by Swissmedic is to ensure that the Swiss Agency for Therapeutic Products receives accurate and timely information about therapeutic products being marketed in Switzerland.
Information such as product name, manufacturer, distributor, ingredients, intended use, adverse reactions, and efficacy data may need to be reported on received by Swissmedic.
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