OIP should start this recirculation procedure within 60 days of adoption of this resolution and should complete the recirculation process within 60 days thereafter.

Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being

in paragraph 1, introductory wording, the words drawing up are replaced by issuing

When new information is received that may impact on the current Safety Specification, Pharmacovigilance Plan or risk minimisation activities Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached

within 60 days of an important (pharmacovigilance or minimisation) milestone being reached

Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being

In addition, an updated RMP should be submitted When new information is received that may impact on the current Safety Specification, Pharmacovigilance Plan or risk minimisation activities Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached At the request of the EMEA.

Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being

In addition, an updated RMP should be submitted when new information is received that may impact on the current Safety Specification, Pharmacovigilance Plan or risk minimisation activities within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached at the request of the EMEA

In addition, an updated RMP should be submitted When new information is received that may impact on the current Safety Specification, Pharmacovigilance Plan or risk minimisation activities Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached At the request of the EMEA

In view of the extension of indication to Restless Legs Syndrome, the periodic safety update reports will be submitted every six months during two years, once a year for the following two years and thereafter at three yearly intervals.

Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being

Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached

I have asked the High Commissioner to submit a plan of action within 60 days.

All countries involved must provide written consent to a notified shipment and have 60 days to do so.

Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached.

In addition, an updated RMP should be submitted When new information is received that may impact on the current Safety Specification, Pharmacovigilance Plan or risk minimisation activities Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached At the request of the EMEA

Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached.

Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached

Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached

The appointment shall be made by the Committee within 60 days at most following receipt of the request.

Within a period of 60 days, his vocabulary went from two to three words to 300 words.

In Article 110(3), the words Article 55(e) are replaced by Article 55(1)(e) .

29 Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached

Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached

Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached.

if the other Party raises objections in writing within that 60 day period, Article 8 shall apply.

An advance of EUR 100000 shall be paid within 60 days after reception of a request of payment by France.

The products to be withdrawn must be removed from intervention stocks within 60 days of the award of the tender to the successful tenderer.

s Evaluation in 30 60 days

You'll get your money in 60 days.

In addition, an updated RMP should be submitted When new information is received that may impact on the current Safety Specification, Pharmacovigilance Plan or risk minimisation activities Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached ''. At the request of the EMEA.

elaborating a common evaluation of the situation and of possible further developments

The chairperson of the arbitration panel shall fix the date and time of the hearing in consultation with the Parties to the dispute and the other members of the arbitration panel, and shall confirm this in writing to the Parties to the dispute.

Within 60 days after having received this formal decree the persons concerned can file a legal suit with the respective court.

Match transaction within days

Match transactions within days

Handle 95 of submissions within 2 days Handle 100 of submissions within 5 days

para 4 introducing an obligation to transmit the evaluation reports of the operations to the Management Board within 60 days following the end of an operation

It aims to execute approved payments within a maximum of five days within the UK and within 10 days for other Member States.

To meet its purpose , as many of the indicators as possible should be monthly and ideally released with a timeliness of approximately 30 days ( and 45 60 days for quarterly indicators ) .

35 At the request of the EMEA

In addition, an updated RMP should be submitted When new information is received that may impact on the current Safety Specification, Pharmacovigilance Plan or risk minimisation activities Within 60 days of an important (pharmacovigilance or risk minimisation) milestone being reached At the request of the EMEA

Member States or any person may for a period of 60 days following reception of an application submit comments in writing to the Commission.

Estimates for 1998 are also made uncertain because of questions relatingto the real impact of arbitration once the decentralised system becomes systematic