Article R5132-1-23
The personal data recorded in the processing is kept for a period of twenty-four months from the date of completion of the pathway to integration through economic activity, or from the date of collect…
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Showing 5421–5430 of 53810 articles for “Art. R 418-2”
The personal data recorded in the processing is kept for a period of twenty-four months from the date of completion of the pathway to integration through economic activity, or from the date of collect…
Provided that the employer's situation and the applicable regulations remain unchanged, the position taken by the association mentioned in article L. 5214-1 is valid for five years from the date of no…
If the regional inter-professional joint committee certifies that the employee's career plan is genuine and serious, the employee has six months from notification of the decision to submit an applicat…
Professionals from other Member States of the European Union or the European Economic Area who have been granted partial access to the practice of the profession of physiotherapist under article L. 40…
Professionals from other Member States of the European Union or the European Economic Area who have been granted partial access to practise the profession of chiropodist in France under article L. 400…
When a regional or inter-regional council of the professional body finds that there is an objective reason likely to call its impartiality into question, on receipt of an application, it will immediat…
Professionals who have obtained authorisation to practise part of the profession concerned appear on a separate list containing the professional title under which they are authorised to practise and t…
Where an application for marketing authorisation in France is made for a medicinal product which has already been authorised or is the subject of an application for marketing authorisation currently b…
Except where there is a risk to patients' health, the proprietary medicinal products mentioned in b of 5° of Article L. 5121-1 which are presented in a modified-release oral pharmaceutical form differ…
When an application for authorisation concerns a generic medicinal product of a reference medicinal product which has not been authorised in France, the applicant must indicate the Member State of the…
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