European Medicines Agency/International Federation for Animal Health Europe info day 2014

EventCorporateMedicines

Danish is available via eTranslation, the European Commission's machine translation service.

Translate to Danish | Important information about machine translation

Date

Torsdag, 13 marts 2014, Hele dagen

Placering

European Medicines Agency, Amsterdam, the Netherlands

The info day covers latest developments in the scientific review, legislation and marketing authorisation procedure. It is an opportunity for professionals to receive first-hand information on current developments in the regulatory scene. Registration closed.

Documents

Registration form - European Medicines Agency/International Federation for Animal Health Europe info day 2014

English (EN) (155.73 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Agenda - European Medicines Agency/International Federation for Animal Health Europe info day 2014

English (EN) (86.37 KB - PDF)

Først publiceret: Senest opdateret:
Vis

European Medicines Agency/International Federation for Animal Health Europe info day 2014 announcement

English (EN) (154.87 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - CVMP work plan 2014 (Anja Holm)

English (EN) (948.46 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Pharmacovigilance: Vision and needs for the future (Karen Quine)

English (EN) (732.43 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Pharmacovigilance – vision and needs for the future: EMA perspective (Jos Olaerts)

English (EN) (797.2 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Upcoming actions for the implementation of Regulation (EC) 470/2009 (MRL-Regulation) (Mario Nagtzaam)

English (EN) (275.21 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Consumer safety issues - Approach for injection site residues (Bruno Urbain)

English (EN) (196.68 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Demonstration of efficacy for veterinary medicines containing antimicrobials (Gesine Hahn)

English (EN) (146.26 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Guidance on user safety evaluation for pharmaceutical veterinary medicinal products – development of existing and future guidance (Nicholas Jarrett)

English (EN) (138.96 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Clarification of MUMS policy (David Murphy)

English (EN) (146.18 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Minor Use / Minor Species policy industry feedback (Alexander Bà¶ttner)

English (EN) (229.03 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Packaging and labelling (Johann M. Lenhardsson)

English (EN) (717.63 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Pre-submission phase and guidance for novel products (Fia Westerholm, Nikolaus Kriz)

English (EN) (982.58 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Scanning the horizon - a regulatory perspective (David Mackay)

English (EN) (149.65 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Variations and progress in worksharing (Melanie Leivers)

English (EN) (1.24 MB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Variations - progress in worksharing CMDv comments (Esther Werner)

English (EN) (118.14 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - Impact on administrative burden and fees (Rose-Marie Molina)

English (EN) (236.24 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - EU Telematics strategy for veterinary medicines - Status update (David Mackay)

English (EN) (298.76 KB - PDF)

Først publiceret: Senest opdateret:
Vis

Presentation - EMA new premises (Agneta Brandt)

English (EN) (2.98 MB - PDF)

Først publiceret: Senest opdateret:
Vis

Share this page