Examples of using It shall forthwith inform in English and their translations into Slovak
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It shall forthwith inform the Commission and the other Member States thereof.
When a country of destinationgrants a general authorisation under paragraph 1, it shall forthwith inform the other Member States and the Commission thereof.
It shall forthwith inform the Commission thereof, and paragraph 2 shall apply.
Where a Member Stategrants an exemption provided for in paragraph 1, it shall forthwith inform the competent authorities of the other Member States and the Commission thereof.
It shall forthwith inform the Commission and the other Member States thereof.
Where a Member Stategrants an exemption provided for in paragraph 1, it shall forthwith inform the competent authorities of the other Member States and the Commission of the exemptions it has granted.
It shall forthwith inform the other Member States and the Commission of any such withdrawal.
If it encounters obstacles in furnishing the information orif it refuses to furnish the information, it shall forthwith inform the requesting authority to this effect, indicating the nature of the obstacles or the reasons for its refusal.
It shall forthwith inform the other Member States and the Commission of any such withdrawal.
Where, after that consultation,the Commission establishes that the measure is unjustified it shall forthwith inform the Member State that has taken the initiative and the manufacturer or his authorised representative established within the Community thereof.
It shall forthwith inform the other Member States and the Commission of any such withdrawal of a recognition.
Where, following consultation with the parties concerned,the Commission establishes that the measure is unjustified, it shall forthwith inform the Member State concerned, as well as the manufacturer or its authorised representative established within the Community and the other Member States.
It shall forthwith inform the other Member States and the Commission of any such withdrawal of a notification.
Should a Member State consider that, in respect of a person holding an authorization granted by another Member State under the terms of paragraph 1, the conditions of authorization are not,or are no longer met, it shall forthwith inform the Commission and the other Member State involved.
It shall forthwith inform the other Member States and the Commission thereof, stating the reasons on which its decision is based.
Where a Member State considers that there are grounds for supposing that the marketing authorisation of the medicinal product concernedmay present a risk to public health, it shall forthwith inform the applicant, the reference Member State which granted the initial authorisation, any other Member States concerned by the application and the Agency.
If at any time a Contracting State decides not to require prior written consent, either generally or under specific conditions, for transit transboundary movements of hazardous wastes or other wastes,or modifies its requirements in this respect, it shall forthwith inform the other Contracting States of its decision.
Where a Member State considers that there are grounds for supposing that the marketing authorization of the veterinary medicinal product concerned may present a risk to human or animal health orthe environment, it shall forthwith inform the applicant, the reference Member State, any other Member States concerned by the application and the Agency.
If at any time a Party decides not to require prior written consent, either generally or under specific conditions, for transit transboundary movements of hazardous wastes or other wastes,or modifies its requirements in this respect, it shall forthwith inform the other Parties of its decision pursuant to Article 13.
Where, as a result of the evaluation of pharmacovigilance data, a Member State considers that a marketing authorisation should be suspended,withdrawn or varied in accordance with the guidance referred to in Article 106(1), it shall forthwith inform the Agency, the other Member States and the marketing authorisation holder.
Where, as a result of the evaluation of veterinary pharmacovigilance data, a Member State considers that a marketing authorization should be suspended, withdrawn or varied to restrict the indications or availability, amend the posology,add a contraindication or add a new precautionary measure, it shall forthwith inform the Agency, the other Member States and the marketing authorization holder.