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Media Release Basel, 20 November 2009 European medical advisory committee does not recommend approval of for deadly form of brain cancer Roche (SIX: RO, DOG; OT CQX: RUGBY) announced today that the
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The European Medical Advisory Committee is an official body established by the European Medicines Agency (EMA) to provide scientific advice and recommendations on medicines for human use.
Companies or individuals seeking scientific advice or recommendations on medicines for human use are required to file the European Medical Advisory Committee.
To fill out the European Medical Advisory Committee, companies or individuals need to submit a formal application providing detailed information about the medicine, research data, proposed indication, and specific questions to be addressed.
The purpose of the European Medical Advisory Committee is to assist companies or individuals in obtaining scientific advice and recommendations to support the development and approval of medicines for human use.
When filing the European Medical Advisory Committee, companies or individuals are required to provide information on the medicine, research data, proposed indication, specific questions, and any relevant supporting documentation.
The deadline to file the European Medical Advisory Committee in 2023 has not been specified. It is recommended to refer to the official guidelines or contact the European Medicines Agency (EMA) for the most up-to-date information.
The penalty for the late filing of the European Medical Advisory Committee may vary depending on the specific circumstances and regulations of the European Medicines Agency (EMA). It is advisable to consult the official guidelines or contact the EMA for detailed information regarding penalties.
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