Due to the sensitive nature of pharmaceutical cleanrooms, cleaning and disinfection takes on a higher level of importance, and disinfectant validations are critical to ensure that regulatory standards are met.

Here Tim Sandle takes us through the best practices for cleaning and disinfecting, topics including:

- Global guidelines for disinfection in cleanrooms: EU GMP (& draft Annex 1), USP [1072], FDA aseptic processing guidance, PIC/S
- Importance of cleaning and disinfecting
- How to select disinfectants
- How to use disinfectants effectively
- Points for success
- Approaching disinfectant validation
- Practical approach to disinfectant validation
- Legal requirements for disinfectants

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