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Showing 191–200 of 47948 articles for “Art. R 232-3”
All the medical examinations and documents required to examine the authorisation application are at the applicant's expense. The applicant pays a flat-rate contribution to the costs of this investigat…
The samples are sent to the laboratory used in a form that respects anonymity. The analyses are carried out in accordance with international standards. With the exception of substances for which a dec…
A Scientific Steering Committee is set up within the Agency to assist it with scientific matters. To this end: 1° Each year, it proposes to the College at least one call for research projects relating…
From the moment the person concerned is notified of the decision ordering the test until the end of the sampling and screening operations, the person tested remains accompanied at all times by the per…
The French Anti-Doping Agency is authorised to create an automated personal data processing system to facilitate the exchange of information relating to Therapeutic Use Exemptions between this Agency,…
The head of the medical department of the Agence française de lutte contre le dopage, deputised where necessary by the scientific adviser to the President of the Agency, is responsible for compliance…
The information and personal data recorded in the automated processing may not be kept for more than eighteen months from the expiry of the period of validity of the authorisation. However, in the eve…
The Sanction Committee shall issue a reasoned decision. The decision is signed by the chairman of the panel. It is notified by registered letter with acknowledgement of receipt or by letter delivered…
The blood sample is transported and analysed in accordance with international standards.
Where an Athlete is sanctioned for an anti-doping rule violation based on an Adverse Analytical Finding, the Athlete's biological profile shall be restored to its original state at the start of the Pr…
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