News and Events

Please check back frequently for the latest news and press releases regarding STERIS Life Sciences products and solutions.

ispe nordic advanced aseptic processing conference in denmark, current trends and advanced technology used in aseptic processing

october 7th, 2015 at 09:00 to 17:00

steris life sciences senior product manager, juha mattila, will be speaking at the advanced aseptic processing conference. the conference will give you the latest trends in processes and equipment for aseptic processing including discussions on isolators/rabs, single-use equipment, containment, case stories and more.

interphex cleaning validation considerations for continuous manufacturing processes

october 15th, 2015 – 4:00-5:00 pm

steris life sciences manager of technical services, paul lopolito, and technical services specialist, elizabeth rivera, will be presenting continuous manufacturing focuses on streamlining production while minimizing the process footprint and waste from non-value activities.

vhp process with vacuum pulses for small lumen medical devices or blister packed goods

november 17th, 2015 at 8:00-17:00

steris life sciences senior product manager, juha mattila, will be speaking in budapest hungary at a steris dealer organized one-day conference along with gerhard lauth and mauro perotti. he will be discussing low temperature terminal sterilization applications (lts-v) with vaporized hydrogen peroxide vhp®.

join steris life sciences at achema 2015 for a speaker session
  • wednesday, june 17 11:30am- on-line toc monitoring in gmp parts washers (olivier van houtte, marcel dion, and george verghese) hall 11.0 granat
  • wednesday, june 17 12:00pm- compatibility of materials and wall coatings for vhp decontamination (gerhard lauth) forum, level 1 in room panorama 3
  • wednesday, june 17 12:10pm- advantages and applications of vhp low temperature terminal surface sterilization for pharmaceutical manufacturing process and products (juha mattila) hall 3 via west, facette
  • thursday, june 18 3:00pm- automated washing principles and common mistakes (olivier van houtte and paul lopolito) forum, level 1 in room panorama 1
  • thursday, june 18 4:30pm- clean room requirements for optimal decontamination with vaporized h2os (gerhard lauth) forum, level 1 in room panorama 1
  • thursday, june 18 5:00pm- biofilm remediation strategies (paul lopolito) illusion 2, cmf
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

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

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