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Swissmedic clinical trial notification forms

Name: Swissmedic clinical trial notification forms

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Language: English

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This site and the enclosed links contain useful information for sponsors, investigators or research institutions conducting clinical trials with medicinal products in.

Clinical trials may only be carried out in Switzerland if they have been approved by a Cantonal Ethics Committee, upon which Swissmedic is notified and is. For further instructions on the use of this form, please read the information provided on our web page kaichaemyren.space trials in the “Guidelines for.

, CTAs for categories B and C clinical trials can be made in parallel to on paper and CD (including cover letter and application form) in accordance with. BW_10_e_FO Application Form for clinical trials on medicinal products relating to clinical trials - Compulsory notification (PDF, kB, ). Please submit all documents on paper and CD (including the form) in There is no specified binder colour for earlier clinical trials or for collective submissions.

Documents and forms Veterinary medicines · Complementary medicinal product · Herbal medicinal · Official Control Authority Batch Release · Authorizations /.

Other trials with medical devices only require the authorisation of the Cantonal Ethics Committee (category A clinical trials) and do not need to. Swissmedic • Hallerstrasse 7 • Berne • kaichaemyren.space • Tel. .

Form BW_10_e_FO Reporting Related to a Clinical Trial. Swissmedic is responsible for the authorization of health products, and for licensing their manufacturing and wholesale.

It also deals with clinical trials.


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