Join Vaisala Regulatory Expert Piritta Maunu as she discusses methods of stability testing in drug production and how they relate to monitoring. Piritta will outline five practical tips for better stability monitoring, including: requirements of stability studies, best practices for mapping qualification studies, proper use of mean kinetic temperature, proper response to incidents and OOS cases, and ensuring accurate RH % measurements.
- Background on Stability testing
- Regulatory Requirements
- Manual or Automatic Monitoring?
- Five Practical Tips
Who should attend
- Quality Assurance & Quality Control personnel
- Laboratory managers & technicians
- Facility managers
- Regulatory & compliance personnel
- Pharmaceutical Scientists
- Manufacturers of raw material and ingredients
Piritta Maunu has 15 years of experience in biotechnology, having worked in several quality management positions. Maunu holds a degree of M.Sc. (Cell Biology) and is certified to teach with a specialty in General Biology, both degrees from the University of Jyväskylä, Finland. In her role at Vaisala, she supports the sales department, assists the quality department with audits, creates educational content for life science customers, and provides application support to R&D teams creating solutions for monitoring critical environments.