消毒资格

You need confidence in the ability of your anti微生物 products and procedures to eliminate contaminants in your facility. With more than 30 years of experience performing disinfectant efficacy studies and 消毒资格 studies, 我们有经验的, consultative team will partner with you to ensure safety is never compromised.

Disinfectant efficacy and disinfectant qualification for controlled manufacturing environments 

Disinfection qualification formally evaluates the efficacy and suitability of anti微生物 products and procedures used to eliminate contaminant microorganisms and viruses on various surface types and components within an aseptic, 无菌 or otherwise controlled manufacturing environment. 使用GLP方法, disinfectant efficacy testing formally evaluates the efficacy and suitability of anti微生物 products used to eliminate contaminant microorganisms on various surface types and components.

元件符合 USP <1072> disinfectant qualification methods and will partner with you to help you develop an effective cleaning/disinfection regimen for your controlled spaces. 我们可以测试你的表面, using the application methods and products that will be used in your facility against Sponsor provided or im体育APP acquired microorganisms and viruses to generate data to support your practices. Our disinfectant efficacy studies evaluate the effectiveness of disinfectants used in your facilities and provide you with solid GLP or cGMP data.

如欲了解更多有关我们的服务， im体育APP 今天. 

Disinfectant qualification test methods

Disinfectant Qualification for Bacteria, Yeast, and Spores - Representative surfaces found in the GMP manufacturing facility are inoculated with test organisms utilized in the manufacturing production plus any routine microbiological contaminants isolated by the facility during the manufacturing process. The surfaces are disinfected using the disinfection practices commonly used at the facility. 治疗后, the surfaces are assayed for surviving organism. The level of reduction deemed necessary for appropriate disinfection is determined by the GMP facility performing the qualification testing.

Disinfectant Qualification 测试 for Antiviral Activity - Representative surfaces found in the GMP manufacturing facility are inoculated with test viruses utilized in the manufacturing production plus any routine viral contaminants isolated by the facility during the manufacturing process. The surfaces are disinfected using the disinfection practices commonly used at the facility. 治疗后, the surfaces are assayed for surviving viruses by an assay method specific for the test virus. The level of reduction deemed necessary for appropriate disinfection is determined by the GMP facility performing the qualification testing.

Disinfection qualification for the pharmaceutical industry 

使用cGMP方法, im体育APP's anti微生物 experts evaluate the efficacy and suitability of anti微生物 products and procedures used to eliminate contaminant microorganisms on various surfaces and items within an aseptic, 无菌 or controlled manufacturing environment. Our comprehensive 消毒资格 services comply with USP <1072> 消毒资格 methods. Our consultative team will partner with you to develop an effective cleaning regimen for your controlled manufacturing spaces. 

如欲了解更多有关我们的服务， im体育APP 今天.

im体育APP优势

Partner with im体育APP 今天 to ensure the safety of aseptic, 无菌, and controlled environments with our comprehensive 消毒资格 services. With more than 30 years of experience serving as the premier partner to manufacturing organizations with controlled environments, our disinfectant efficacy studies evaluate the effectiveness of disinfectants and procedures used in facilities and provide solid GLP or cGMP data.

To learn more about our 消毒资格 services, learn about additional methods available or to speak with an expert, 与我们联系 今天.