• Hands-on study of wet granulation processes and their possible effects on compression.
• Study and optimization of the critical variables of each technology, process control, granule characterization, impact on compression, troubleshooting and formulation optimization.
• Batches will be granulated in a fluid bed and in a high-shear granulator.

Aimed at

• The pharmaceutical industry and related industries where compliance with GMP standards is required.
• Staff from Development (R&D), Production, Industrialization and Quality departments.

Registration

• Price: €740 + VAT, including attendance, catering, course materials and lunch.
• Due to the limited number of places, bookings will only be confirmed once the registration fee has been paid.
• Certificate of attendance at the end of the session.

Venue

UB-FARMATEC
Campus de la Salud de Bellvitge
Feixa Llarga, s/n
08907 L’ Hospitalet del Llobregat
Barcelona

Speaker

Pablo Martín-Sáiz
Head of Pharmaceutical Development, Ferrer.