Heads of Medicines Agencies: Miscellaneous

1: Home (ALT-H)
2: HMA Joint (ALT-M)
3: Human Medicines (ALT-U)
4: Veterinary Medicines (ALT-V)
- 4.1: Heads of Agencies (ALT-E)
- 4.2: CMDv (ALT-C)
- 4.3: VMRI Product Index (ALT-R)
- 4.4: Directory (ALT-I)

You are here: Veterinary Medicines > CMDv > CMDv guidance > Miscellaneous

4.2.1: About CMDv, Activities (ALT-O)
4.2.2: CMDv guidance (ALT-G)
- 4.2.2.1: General Info on Licensing System (ALT-N)
- 4.2.2.2: Applications (ALT-P)
- 4.2.2.3: Marketing Authorisation procedures (ALT-K)
- 4.2.2.4: Variations (ALT-T)
- 4.2.2.5: Renewals (ALT-W)
- 4.2.2.6: Referrals (ALT-L)
- 4.2.2.7: SPC, Labelling and Package leaflet (ALT-S)
- 4.2.2.8: Miscellaneous
4.2.3: Pharmacovigilance
4.2.4: Reports for Release
4.2.5:
4.2.6: Special topics
4.2.7: Statistics
4.2.8: Calendar
4.2.9: Frequently asked questions (ALT-Q)
4.2.10: Contact Form
4.2.11: submission of translations
4.2.12: What's new Archive (6 months) (ALT-6)

Colostrum and colostrum substitutes

Definition of the term "same medicinal product"

Authorisation of colorants in veterinary medicinal product in the EU

Use of erythrosin in VMP

Q&A 92 Inclusion of non-VMP devices in the packaging

Bee products available in Europe - rev. 4 (Updated 2013)

VMP intended for rabbits

Ectoparasiticidal products for use in animals for consumption and pet animals respectively

Authorisation of ectoparasiticidal collars for companion animals

Pre- dipping requirements

The Reference Member State

Active Substance Master File (ASMF) in the Mutual Recognition and Decentralised Procedures

E-mail use during procedures and standardisation of subheadings

Requirements for starting Material of Biological Origin

Changing the Reference Member State July 2007

EU GMP Guide Part II Basic Requirements for Active Substances used as Starting Materials - GMP compliance for Active Substances