SME applicants currently account for around 10% of centralised marketing-authorisation applications for human medicines and 20% of veterinary applications.
2012 has seen a surge in the number of companies submitting SME declarations to the Agency, with a 48% increase since the end of last year. This indicates a high level of activity in the pharmaceutical sector, but is also a reflection of the new pharmacovigilance legislation coming into operation.
A high proportion of companies registering recently have sought SME status in relation to EudraVigilance, the European Union information system for the management of safety reports. A Medical Dictionary for Regulatory Activities (MedDRA) fee waiver is available to micro and small enterprises, and there are reduced fees for EudraVigilance training for all SMEs.
The majority of registered SMEs (76%) have medicines for human use under development, 4% are developing medicines for veterinary use, 6% are developing products for both human and veterinary use and 14% are service providers.
Further information on the companies registered with the Agency's SME office is available in the publicly available SME register, which has been designed to facilitate and promote interaction amongst SMEs.
Together, the registered SMEs have approximately 2600 medicines at various stages of development. Approximately half of the products developed by SMEs are chemical entities and a quarter are biological medicines, including advanced therapies.
SMEs are strongly encouraged to seek scientific advice on the data required for marketing authorisation for medicines from the Agency early in development. For help and guidance on how to obtain scientific advice, SMEs can turn to the Agency's SME office.