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Manufcature and control of veterinary medicinal products PDF Print E-mail
Written by Petra Müllerová   
The following areas are covered by documents provided in this section:
  • manufacture of veterinary medicinal products including autogenous vaccines
  • manufacture of active substances
  • activities of control laboratories for medicinal products.
This sections is divided into three parts:
  • GMP Guidance documents (EU GMP Guide) and other guidance documents published by the ÚSKVBL according Act No. 378/2007 Coll., on pharmaceuticals
  • Forms and templates
  • Registers and databases (actual registers of manufacturers, control laboratories including scope of activities, register of API manufacturers in the Czech Republic)
Last Updated on Tuesday, 21 March 2017 12:08