Examples of using It shall forthwith inform in English and their translations into Portuguese
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It shall forthwith inform the Commission thereof, and paragraph 2 shall apply.
If a Member State makes use of the options provided for in paragraph 1, it shall forthwith inform the Commission thereof.
It shall forthwith inform the other Member States and the Commission of any such withdrawal.
If a Member State makes use of the options provided for in paragraph 3, it shall forthwith inform the Commission and Member States thereof.
It shall forthwith inform the Commission of any such measure, indicating the reasons for its decision.
In all other cases,the transport undertaking may perform the modified contract; it shall forthwith inform the office of departure of the modification made.
It shall forthwith inform the other Member States and the Commission of any such withdrawal of a notification.
When a country of destination grants a general authorisation under paragraph 1, it shall forthwith inform the other Member States and the Commission thereof.
It shall forthwith inform the Commission and the other Member States of any such withdrawal of notification.
If a Member State makes use of the option provided for in the second subparagraph of paragraph 2, it shall forthwith inform the Commission and the other Member States thereof.
It shall forthwith inform the other Member States and Commission thereof, stating the reasons on which its decision is based.
If the customs authority suspends release of the goods ordetains them in accordance with Article 4 of the basic Regulation, it shall forthwith inform the declarant.
It shall forthwith inform the other Member States and the Commission thereof, stating the reasons on which its decision is based.
A Member State shall withdraw approval from a body which no longer meets the criteria referred to in Annex VII. It shall forthwith inform the Commission and the other Member States thereof.
If the designated authority is not competent to deal with the information demand, it shall forthwith inform the equivalent competent authority of the designated authority that controls or handles the information demanded.
A Member State which has approved a body shall withdraw approval if it finds that the body no longer meets the criteria listed in Annex III. It shall forthwith inform the Commission thereof.
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.
Where a Member State considers that a laboratory within its territory claiming GLP compliance does not in fact comply with GLP to the extent that the integrity orauthenticity of the studies it performs might be compromised, it shall forthwith inform the Commission.
A Member State shall withdraw approval from a body which no longer meets the criteria referred to in Annex VII. It shall forthwith inform the Commission and the other Member States thereof.
Each authority or body which has been designated by the Member States in accordance with Article 2 of Directive 93/5/EEC shall forthwith inform the Commission of the names of the institute orinstitutes which will carry out the tasks referred to in the Annex which have been distributed to it. It shall forthwith inform the Commission of any changes.
Member States shall withdraw notification of a notified body which no longer meets the criteria provided for in Annex V. It shall forthwith inform the Commission and the other Member States thereof.
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 oradd a new precautionary measure, it shall forthwith inform the Agency, the other Member States and the marketing authorization holder.
Where a host Member State adopts a measure pursuant to the second subparagraph orbecomes aware of facts which run counter to these provisions, it shall forthwith inform the Member State where the person concerned is established.
Where a host Member State adopts a measure pursuant to the second subparagraph orbecomes aware of facts which run counter to these provisions, it shall forthwith inform the Member State in which the person concerned is established.
Where a host Member State adopts a measure pursuant to the second subparagraph orbecomes aware of facts which run counter to these provisions, it shall forthwith inform the Member State where the person concerned is established.
Where as a result of the evaluation of adverse reaction reports a Member State considers that a marketing authorization should be varied,suspended or withdrawn, it shall forthwith inform the Agency and the person responsible for placing the medicinal product on the market.
Where a competent authority has objective grounds for considering that the sponsor or the investigator orany other person involved in the conduct of the trial no longer meets the obligations laid down, it shall forthwith inform him thereof, indicating the course of action which he must take to remedy this state of affairs.
Where, as a result of the evaluation of pharmacovigilance data, a Member State considers that a marketing authorisation should be suspended, withdrawn orvaried 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 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 oranimal health or the environment, it shall forthwith inform the applicant, the reference Member State, any other Member States concerned by the application and the Agency.
Notwithstanding Article 17(4), where a Member State considers that there are grounds for supposing that the authorization of the veterinary medicinal produa concerned may present a risk to human oranimal health or the environment(9), it shall forthwith inform the applicant, the Member State which granted the initial authorization, any other Member States concerned by the application and the Committee.