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Oct 6

Development of generics: From R&D to GMP MasterClass

October 6 @ 9:00 am - October 7 @ 5:00 pm

DevofGen oct2020 header nodate

The interface between Development and GMP units is one of the most exciting in the pharmaceutical industry. Mutual understanding of the different regulatory environment and the functional priorities is a key success factor. Conflicts, mostly resulting from different approaches and priorities, can have negative impact on business processes even outside the R&D or GMP areas.

R&D needs flexibility and should not be over-regulated, whereas GMP concentrates on standardization and high throughput. On the other hand, R&D has to create a solid and robust fundament to enable manufacturing and quality control to work according to established and efficient procedures.

The training aims to generate a common understanding of how to best interlink these two areas and create highly efficient processes from product development to routine manufacturing of generic pharmaceutical products.

Venue

online event
Váci út 19. Panorama Office Building
Budapest, 1134
+ Google Map
Phone:
+36 1 848 05 60
Website:
www.glceurope.com

Organiser

GLC europe
Phone:
+36 1 848 05 60
Email:
milu.lal@glceurope.com
Website:
www.glceurope.com

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