How can we address contamination control in rooms at pharmaceutical facilities?
Purpose of the event
- Address the requirements of the new Annex I of the Good Manufacturing Practices with respect to the air conditioning and monitoring of clean rooms
- Propose solutions and tools for their control
Aimed at
- Pharmaceutical industry professionals: facility and process control managers
- Quality assurance officers
Further information
- We will visit the Pharma Lab facilities at TECNALIA. It is necessary to register for the workshop and request the visit.
- Contact: Carmen.martinez@trescal.com
