Du er ikke logget ind
Beskrivelse
Relying on practical examples from the authors’ experience, this book provides a thorough and modern approach to controlling and monitoring microbial contaminations during the manufacturing of non-sterile pharmaceuticals.
Offers a comprehensive guidance for non-sterile pharmaceuticals microbiological QA/QCPresents the latest developments in both regulatory expectations and technical advancementsProvides guidance on statistical tools for risk assessment and trending of microbiological dataDescribes strategy and practical examples from the authors’ experience in globalized pharmaceutical companies and expert networks