Temperature & Humidity Requirements in Pharmaceutical Facilities
Temperature & Humidity Requirements in Pharmaceutical Facilities
Defining room temperature and humidity limits is a frequent topic of debate when designing and operating pharmaceutical and biotechnology facilities. What are appropriate alarm limits and acceptable durations for an alarm condition? Understanding the source of temperature and humidity requirements, and strategies for setting limits, can ensure both compliance and optimum use of energy. This article provides guidance on these topics, with supporting rationales.
Pharmaceutical Graded Space Requirements
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Supplement 6- Annex9- WHO guideline: Temperature and humidity monitoring systems
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Temperature Within The Pharmaceutical Industry
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