Examples of using Post-authorisation in English and their translations into Greek
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Financial
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Official/political
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Computer
There was also a strong increase(over 20%) in post-authorisation activities, and a major rise in the number of referral procedures(77 compared to 55 in 2010).
Based on post-authorisation safety data, there is no
Payments to healthcare professionals for participating in non-interventional post-authorisation safety studies shall be restricted to the compensation for time
This implies that a delegated act is a pre-condition for imposing post-authorisation efficacy studies.
Reports submitted to EudraVigilance include suspected side effects of medicines reported during both the pre- and post-authorisation phases.
Competent authorities should therefore be empowered to impose on the marketing authorisation holder the obligation to conduct post-authorisation studies on safety
contribute to predictability and transparency regarding situations in which post-authorisation studies may be required.
Frequency of undesirable effects for TachoSil based on all adverse event data from six clinical trials, two post-authorisation safety studies
Adverse reactions arising from clinical studies, post-authorisation safety studies and spontaneous reports are
rights of participants in non-interventional post-authorisation safety studies.
Additional safety data include clinical trials, post-authorisation safety studies and post-marketing experience with the mono-components.
prostate tumours must be considered with caution; it will be further investigated in post-authorisation studies.
The focus will also be on stimulating innovation, by establishing a clear legal requirement to conduct post-authorisation safety studies, including those in risk management systems.
Post-authorisation activities relate to variations,
Products for which certain additional information is required post-authorisation, or for which authorisation is subject to conditions
The workload on RMPs will be considerable in the post-authorisation phase, taking into account the need for updates of RMPs agreed at the time of authorisation.
The Agency will review its post-authorisation activities during the ongoing process-improvement exercise to further increase efficiency.
The Agency expects that the number of applications in the post-authorisation area of veterinary medicines will remain largely unchanged.
The following adverse reactions have been identified in two comparative pivotal Phase 3 studies and one post-authorisation study with Sivextro(Table 1).
The number of post-authorisation opinions adopted was also significantly higher(20%)