Human
Standard operation procedure for handling of requests from a national competent authority to the CMDh for a recommendation on the classification of an unforeseen variation under Article 5 of Commission Regulation (EC) No...
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Standard operating procedure for provision of scientific recommendation on classification of advanced-therapy medicinal products
English (EN) (343.23 KB - PDF)
Work instructions for handling of paediatric Article 45 work-sharing procedures by the Co-ordination Group for Mutual Recognition and Decentralised Procedure – Human (CMDh) secretariat
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Work instructions for handling of paediatric Article 46 work-sharing procedures by the Co-ordination Group for Mutual Recognition and Decentralised Procedure – Human (CMDh) secretariat
English (EN) (231.23 KB - PDF)
Standard Operating Procedure for marketing status reporting and sunset clause monitoring (Human Medicine)
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Veterinary
Work instructions for handling of renewals for centrally authorised veterinary medicinal products
Handling of renewals for centrally authorised veterinary medicinal products
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Standard operating procedure on annual re-assessment of centrally authorised veterinary medicinal products under exceptional circumstances
The purpose of this SOP is to provide the project managers and assistants in the Veterinary Medicines
sector with guidance on the procedure to be followed for dealing with annual reassessments for
centrally authorised medicinal products for veterinary use authorised under exceptional circumstances.
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Standard operating procedure for processing of type II variations for medicinal products for veterinary use
English (EN) (207.58 KB - PDF)
Standard operating procedure for type IA variations (single and grouped) to centralised marketing authorisations (medicines for veterinary use)
English (EN) (168.78 KB - PDF)
Standard operating procedure for type IB variations to centralised marketing authorisations (medicines for veterinary use)
English (EN) (181.93 KB - PDF)
Work instructions for marketing status and sunset clause monitoring for centrally authorised veterinary medicinal products
New WIN following revision of IQM structure and simplification of procedure.
English (EN) (90.8 KB - PDF)