Medicamentos huérfanos
Frontiers | RNA-based drugs and regulation: Toward a necessary evolution of the definitions issued from the European union legislation
procedures for medicinal products for human and veterinary use in accordance with Council
The role of specialised agencies in decentralising EU governance | Semantic Scholar
laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and es
Marketing authorization and licensing of medicinal products in EU: Regulatory aspects - ScienceDirect
REGULATION (EC) No 2141/96
Council Regulation (EEC) No 2309/93 of 22 July 1993 laying down Community procedures for the
Regulation No. 726/2004 of the EP and of the Council of 31 March 2004 laying down Community procedures for the authorisation and
PDF) Regulatory review of the environmental risk assessment of veterinary medicinal products in the European Union, with particular focus on the centralised authorisation procedure
Commission communication on the Community marketing authorisation procedures for medicinal products (98/C 229/03) As part of the
Panace@ - Revista de Medicina, Lenguaje y Traducción
Agency's Management Board may, on a proposal from the Executive Director, specify any other provision proving necessary for th
EMA Guidance | ESGCT
Council Regulation amending Regulation (EEC) No 2309/93 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation
Supplementary Protection Certificates Phillip Johnson. - ppt download
The GMA concept and products authorised under the 'old' Regulation (EEC) No 2309/93
COMMISSION DECISION of 12/11/96 granting the marketing authorization for the medicinal product for human use, "HYCAMTIN - T
Clinical Safety Data Management Periodic Safety Update | PDF | Pharmacovigilance | Clinical Trial
Šio darbo tikslas - atlikti kompleksinį ES direktyvos 2001/18/EB dėl genetiškai modifikuotų organizmų apgalvoto išleidimo
Legal Basis, Principles and Organisation of the EU Pharmacovigilance System - Regulatory Pharmacovigilance in the EU | Pharmacovigilance
PDF to HTML - Convert PDF files to HTML files
PDF to HTML - Convert PDF files to HTML files
REGLAMENTO (CEE) N° 2309/93
Legal and Scientific Considerations in Nonclinical Assessment of Biotechnology Products
Overview of Presentation Introduction and Background EU Enlargement EMEA, It's “Euro-partners” and International Network 4
