View pictures of our training event in Istanbul, Turkey, feb 14-16. Michor Consulting presented an overview of biosimilars in the US and EU, and gave an insight into
the quality and GMP of biosimilars.
This Seminar will look at what to expect when the new EU regulation is implemented: The transition period, Effect on Notified Bodies, Impact of the MDR on Quality Management Systems (QMS), technical documentation, clinical trial requirements, UDI and combination products.
Details & booking