Prior to developing the registration dossier

• Procedure Type: National procedures, Mutual Recognition and decentralised procedures
• Type of Application: Full, Generic medicinal products, Hybrid, Well-established use, Informed consent applications
• Active ingredient, dosage form, dosage and indication, target species (veterinary medicines)
• Market research: data protection and patent

During the development of the registration dossier

• Advice during the preparation of the dossier by the Laboratory
• List of questions requested by the Health Authorities

After obtaining authorization

• Modifications to marketing authorization
• Requests for approvals and five yearly renewals
• Post-marketing studies
• PSURs