2014

ivt cleaning validation and critical cleaning process conference
7/16/2014 4:04 PM

august 20, 2014 - 8:30-10:00 am

steris life sciences technical specialist beth kroeger will be presenting best practices for a robust cleaning validation program at ivt’s cleaning validation and critical cleaning process conference taking place in san diego, ca.

establishing limits for cleaning validation
7/1/2014 10:29 AM

july 10, 2014 webinar

noon - 1:30 pm eastern daylight time

cleaning validation is a key part of pharmaceutical, biopharmaceutical, and medical device manufacturing.  one of the critical steps in performing a successful cleaning validation is establishing the limits of residue that can remain on the surface being cleaned.  several factors can impact the selection and validation of these residual limits, such as sampling technique, analytical methodology, and areas of non-uniform contamination.

automated washing basic principles and common mistakes
5/23/2014 8:19 AM

join us for a webinar on may 29

automated washing systems are often used for critical cleaning and drying applications in research, pharmaceutical and biopharmaceutical manufacturing facilities. typical applications include cleaning of laboratory glassware and parts from equipment used in the manufacturing process of injectable, oral liquid and solid dosage drugs.

rouging in pharmaceutical and biopharmaceutical manufacturing systems
5/22/2014 9:02 PM

june 5, 2014 webinar

12 pm - 1:30 pm edt

most pharmaceutical and biotech companies experience some corrosion and rouging of their stainless steel surfaces. rouge can often be found in high purity water and steam systems as well as process equipment exposed to corrosive environments.

preventing and correcting microbial contamination of process equipment
3/21/2014 8:00 AM

april 3, 2014 webinar

noon - 1:30 pm eastern standard time

microbial contamination of process equipment is a concern for pharmaceutical, biopharmaceutical, medical device, dietary supplement and personal care industries. microbial contamination issues can lead to delays in manufacturing and product release.

new vaprox training and certification course
3/13/2014

the vhp marketing team is proud to announce the launch of our new vaprox us epa label training and certification website.

besuchen sie unser seminar grundlagen der reinigung und reinigungsvalidierung in gmp
2/6/2014 9:46 AM

die steris corporation ist der branchenweit führende anbieter von lösungen zur reinigung, reinigungsvalidierung und mikrobiellen kontrolle in der pharmaindustrie. unser expertenteam hält seit über 20 jahren erfolgreich fachseminare und -vorträge, in denen anhand von cgmp-standards (current good manufacturing practice) und praxiserfahrungen die herausforderungen regulierter branchen bei reinigung, reinigungsvalidierung und mikrobieller kontrolle erläutert werden.

establishing limits for cleaning validation
2/6/2014 3:10 PM

february 19, 2014 webinar

noon - 1:30 pm eastern standard time

cleaning validation is a key part of pharmaceutical, biopharmaceutical, and medical device manufacturing. one of the critical steps in performing a successful cleaning validation is establishing the limits of residue that can remain on the surface being cleaned. several factors can impact the selection and validation of these residual limits, such as sampling technique, analytical methodology, and areas of non-uniform contamination.

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