Examples of 'authorisation applications' in a sentence
Meaning of "authorisation applications"
This phrase relates to the process of submitting or applying for authorizations. It pertains to formal requests or paperwork seeking permission, approval, or legal rights to carry out specific actions, operations, or activities as required within the relevant jurisdiction
How to use "authorisation applications" in a sentence
Basic
Advanced
authorisation applications
Before marketing authorisation applications are submitted.
Protocol assistance procedures on future marketing authorisation applications.
Number of marketing authorisation applications for advanced therapy products.
Requirements for specific marketing authorisation applications.
Authorisation applications are made for one or several specific uses.
Number of marketing authorisation applications granted.
Number of requests for accelerated assessment of marketing authorisation applications.
Mixed marketing authorisation applications.
Authorisation applications is expected.
Clinical trial authorisation applications.
Requirements for abridged and reduced dossiers for marketing authorisation applications.
All fishing authorisation applications shall be accompanied by the following documents.
Risk management plans are required for all new marketing authorisation applications.
Prefectural authorisation applications for the use of video protection devices.
The medicine market itself determines the rate of inspections resulting from authorisation applications and variations.
See also
authorisation and supervision
authorisation application
authorisation code
authorisation for placing
authorisation application
authorisation code
authorisation for placing
Requirements for marketing authorisation applications for particular veterinary medicinal products.
EMA launches checklist to facilitate validation for initial marketing authorisation applications.
Two marketing authorisation applications for veterinary vaccines were also examined at that time.
Annex I List of nationally authorised medicinal products and marketing authorisation applications.
Manufacturing sites listed in new marketing authorisation applications have already been inspected in connection with.
Authorisation applications must be addressed to the Tax Administration.
S Marketing authorisation applications.
Guideline on the non-clinical documentation for mixed marketing authorisation applications.
Marketing authorisation applications for new medicines should contain impact studies of their effects upon biodiversity.
Management and follow-up of marketing authorisation applications under the centralised procedure.
Marketing authorisation applications for which no alternative bioequivalence data or a justification was submitted ( annex IB ).
The success rate for the marketing authorisation applications is assumed to be around 80.
Marketing authorisation applications are on going in other countries, including Australia and Switzerland.
For vaccines - Review the quality aspects of marketing authorisation applications for biological and biotechnological medicinal.
Figures on authorisation applications for clinical trials in Switzerland, including the number of refusals ;.
EMA has encouraged the formation of multinational assessment teams since 2013 for initial marketing authorisation applications.
An analysis of marketing authorisation applications via the mutual recognition and decentralised procedures in Europe.
Furthermore, this indication should not be granted for the pending marketing authorisation applications ( see Annex I ).
Marketing authorisation applications have been filed in Europe and Japan.
The statutory time limit for assessing these marketing authorisation applications will be reduced from 210 - 150 days.
Marketing authorisation applications Protocol assistance Inspections.
New format requirements for marketing authorisation applications from 1 January 2018.
Authorisation applications concerning railways, waterways, motorways, federal, state and district road, etc.
SSA does now accept receiving your authorisation applications and declarations of receipts via e-mail.
Guidelines for marketing authorisation applications under the National, Mutual Recognition and Decentralised procedures.
ECHA has launched consultations on 17 authorisation applications for uses of trichloroethylene ( TCE ).
Examination of authorisation applications under Article 20.
Initial marketing authorisation applications per therapeutic area in 2004.
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