Use of high potency active pharmaceutical ingredients (HPAPIs) is increasing as pharmaceutical companies focus on developing more effective, better targeted medicines. This growing interest is increasing demand for the specialist handling and containment systems needed to ensure such products can be manufactured in a manner that complies with employee safety regulations. In addition, the trend has prompted manufacturers to search for faster, less labor intensive ways of verifying the efficacy of their containment systems. As a result, the interpretation of containment verification data has become a major focus for internal teams at drug companies and contract manufacturing organizations (CMOs). Click Here For Complete Abstract Text
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