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Market Applications

  • Pharmaceutical Manufacturing

    Custom solutions for producers of active pharmaceutical ingredients (API) or finished pharmaceuticals such as tablets, capsules, liquid doses, and parenterals.

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  • Biotechnology

    Custom solutions for the formulation and fill of drugs, vaccines, and therapeutics in a variety of dosage forms in small or large batch production.

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  • Research and Laboratory

    Custom solutions for contamination control in research using rodents, small animals and primates to get your results to the marketplace faster.

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  • Medical Devices

    Custom solutions for disinfecting or sterilizing your FDA Class 1, Class 2, or Class 3 devices from implantable joints to sterilized IV bags.

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  • Cosmetics

    Custom solutions to help maintain a clean and controlled environment during the manufacturing of cosmetic products.

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  • Dietary Supplements

    Custom solutions for contamination control during the manufacturing of high quality dietary supplements to help ensure product safety.

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Recent News

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.

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.

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.

reinigungsvalidierung im gmp bereich
11/15/2013 1:36 PM

steris life sciences auf dem seminar der swiss cleanroom concept (scc): „reinigungsvalidierung im gmp bereich“

steam sterilization principles
11/11/2013 4:00 PM

the article presents how a good understanding of basic steam sterilization principles can help with avoiding most common mistakes made when using steam autoclaves.

use of hydrogen peroxide vapor biodecontamination technology for facility commissioning
11/4/2013 9:38 AM

this article discusses the successful use of hydrogen peroxide vapor in the biodecontamination of a new 120,000+ ft3 lab animal research facility for the purpose of a facility commissioning process.1 it will discuss the reasons why this process was chosen; the preparation of the facility; the execution of the biodecontamination; and the results.

an audit approach to address microbial contamination in process equipment
10/10/2013 1:00 PM

paul lopolito, technical service manager for steris life sciences, is presenting at the interphex puerto rico 2013 conference!

join paul for his presentation: an audit approach to address microbial contamination in process equipment.

current issues in medical device sterilization
10/1/2013 8:00 AM

join steris at walt disney world's disney's yacht club resort for a tech team seminar on topics critical to success in medical device sterilization. in this two-day event, industry experts will help attendees gain an in-depth understanding of the relationship between sterilization and medical device design, validation, manufacturing and packaging

solutions to rouge and stainless steel maintenance
9/25/2013 11:00 AM

join steris corporation's mike gietl and paul lopolito for a live interactive webinar on solutions to rouge and stainless steel maintenance.

preventing and correcting microbial contamination of process equipment
9/11/2013 12:00 PM

join steris corporation's paul lopolito and elizabeth rivera for a live interactive webinar where they will discuss preventing and correcting microbial contamination of process equipment.

steris technical expert presenting at the cleaning validation conference
8/20/2013 1:30 PM

paul lopolito, technical services manager at steris, will be presenting on "design of a cleaning and passivation program for buufer preperation tanks" at the cleaning validation conference in philadelphia, pa.

establishing limits for cleaning validation
6/27/2013 12:00 PM

join steris corporation's paul lopolito (technical services manager) and michael gietl (global product manager) for a 90 minute interactive webinar on establishing limits for cleaning validation, hosted by executive conference.

validation and performance testing of antimicrobial technologies
6/24/2013 12:00 PM

join steris corporation's jim polarine (technical services manager) for an interactive webinar as he discusses validation and performance testing of antimicrobial technologies.

solutions for addressing bacterial spore and mold spore excursions
6/21/2013 12:00 PM

steris corporation's jim polarine (technical services manager) will be presenting on solutions for addressing bacterial spore and mold spore excursions in pharmaceutical and biotech operations at the pda texas chapter's all day event in june.

rouging in pharmaceutical and biopharmaceutical manufacturing systems
6/19/2013 12:00 PM

join steris corporation's paul lopolito (technical services manager) for an interactive webinar as he discusses rouging in pharmaceutical and biopharmaceutical manufacturing systems.

an eco friendly assessment of cleaning agents in gmp regulated facilities
6/1/2013 8:00 AM

steris corporation's elizabeth rivera discusses cleaning agents used in gmp applications in the may / june issue of pharmaceutical engineering's digital magazine.

pda midwest meeting
5/2/2013

steris corporation's paul lopolito will provide an overview of cleaning validations at the pda midwest chapter dinner meeting in chicago.

steris at interphex 2013 in new york city
4/23/2013

it happens at interphex! join us this april 23-25 at the javits center in new york city for the leading annual pharmaceutical and biopharmaceutical trade show. steris life sciences combines formulated chemistries, engineered products and services for contamination control in the biopharmaceutical markets. we help our customers to increase their productivity, efficiency and operational excellence while maintaining regulatory compliance. come to interphex and visit us at booth# 3121!

steris life sciences scholarship recipients named
4/10/2013 3:12 PM

btec is pleased to announce that steris life sciences has established two annual scholarships to benefit students taking btec courses. the initial recipients of these scholarships are chloe grogan and raul doyle, who received the awards this semester.

grundlagen der reinigung und reinigungsvalidierung
3/15/2013 8:30 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 nichtkommerzielle seminare und präsentationen, in denen anhand von cgmp-standards (current good manufacturing practice) und praxiserfahrungen die herausforderungen regulierter branchen bei reinigung, reinigungsvalidierung und mikrobieller kontrolle thematisiert werden. in diesem seminar werden branchenspezifische beispiele und praktische einblicke in die entwicklung wirksamer reinigungsprogramme vorgestellt. zudem erhalten die teilnehmer einen überblick über einschlägige regulatorien sowie praktische informationen zur validierung wirksamer reinigungsprogramme. der schwerpunkt des seminars liegt auf der reinigung von prozessanlagen und der reinigungsvalidierung.

grundlagen der reinigung und reinigungsvalidierung
3/13/2013 8:00 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 nichtkommerzielle seminare und präsentationen, in denen anhand von cgmp-standards (current good manufacturing practice) und praxiserfahrungen die herausforderungen regulierter branchen bei reinigung, reinigungsvalidierung und mikrobieller kontrolle thematisiert werden. in diesem seminar werden branchenspezifische beispiele und praktische einblicke in die entwicklung wirksamer reinigungsprogramme vorgestellt. zudem erhalten die teilnehmer einen überblick über einschlägige aufsichtsrechtliche leitlinien sowie praktische informationen zur validierung wirksamer reinigungsprogramme. der schwerpunkt des seminars liegt auf der reinigung von prozessanlagen und der reinigungsvalidierung.

gaining and re-establishing control of your cleanroom
1/9/2013 1:00 PM

led by steris corporation's jim polarine. this 90-minute webinar will focus on the critical steps in starting up a new cleanroom operation and releasing it for manufacturing. it includes a case study-based approach to dealing with excursion events and establishing control of the cleanroom after a worst case event.

seminar basic concepts in cleaning and cleaning validation for gmp regulated industries
10/11/2012
steris corporation (www.sterislifesciences.com) is the industry leader in providing cleaning, cleaning validation and microbial control solutions to the pharmaceutical manufacturing industry. for over 20 years our team of experts has provided non-commercial seminars and presentations based on both current good manufacturing practices and on real-world experience in addressing the cleaning, cleaning validation and microbial control challenges of regulated industries. this seminar will provide industry examples and real-world insights into development of robust cleaning programs, and will provide both a review of relevant regulatory guidance as well as practical information on validation of robust cleaning programs. the focus of this seminar will be processing equipment cleaning and cleaning validation.

seminar basic concepts in cleaning and cleaning validation for gmp regulated industries
10/9/2012
steris corporation (www.sterislifesciences.com) is the industry leader in providing cleaning, cleaning validation and microbial control solutions to the pharmaceutical manufacturing industry. for over 20 years our team of experts has provided non-commercial seminars and presentations based on both current good manufacturing practices and on real-world experience in addressing the cleaning, cleaning validation and microbial control challenges of regulated industries. this seminar will provide industry examples and real-world insights into development of robust cleaning programs, and will provide both a review of relevant regulatory guidance as well as practical information on validation of robust cleaning programs. the focus of this seminar will be processing equipment cleaning and cleaning validation.

seminar basic concepts in cleaning and cleaning validation for gmp regulated industries
9/20/2012

steris corporation (www.sterislifesciences.com) is the industry leader in providing cleaning, cleaning validation and microbial control solutions to the pharmaceutical manufacturing industry. for over 20 years our team of experts has provided non-commercial seminars and presentations based on both current good manufacturing practices and on real-world experience in addressing the cleaning, cleaning validation and microbial control challenges of regulated industries. this seminar will provide industry examples and real-world insights into development of robust cleaning programs, and will provide both a review of relevant regulatory guidance as well as practical information on validation of robust cleaning programs. the focus of this seminar will be processing equipment cleaning and cleaning validation.

seminar basic concepts in cleaning and cleaning validation for gmp regulated industries
9/18/2012

steris corporation (www.sterislifesciences.com) is the industry leader in providing cleaning, cleaning validation and microbial control solutions to the pharmaceutical manufacturing industry. for over 20 years our team of experts has provided non-commercial seminars and presentations based on both current good manufacturing practices and on real-world experience in addressing the cleaning, cleaning validation and microbial control challenges of regulated industries. this seminar will provide industry examples and real-world insights into development of robust cleaning programs, and will provide both a review of relevant regulatory guidance as well as practical information on validation of robust cleaning programs. the focus of this seminar will be processing equipment cleaning and cleaning validation.

vhp seminar
9/10/2012

teilnehmergebühr: die teilnehmergebühr für dieses seminar beträgt € 575,00 zzgl. mwst. und beinhaltet die tagungsunterlagen auf usb-card, zwei mittagessen, ein gemeinsames abendessen an bord eines ausflugschiffes sowie pausenverpflegung während der veranstaltung am 10. und 11. sept. 2012 während der veranstaltung.
seminar stornierungskosten:
• 6 wochen vor seminarbeginn kostenfrei
• 4 wochen vor seminarbeginn 50%
• 2 wochen vor seminarbeginn 100%
• ersatzteilnehmer werden ohne zusätzliche kosten akzeptiert

bitte reservieren sie ihre übernachtung direkt im veranstaltungshotel mit hinweis auf das stichwort “steris seminar“.
http://www.netinform.de/veranstaltungen/pdf/steris-vhp-seminar.pdf

basic concepts in cleaning and cleaning validation for gmp regulated industries
7/12/2012

steris corporation (www.sterislifesciences.com) is the industry leader in providing cleaning, cleaning validation and microbial control solutions to the pharmaceutical manufacturing industry. for over 20 years our team of experts has provided non-commercial seminars and presentations based on both current good manufacturing practices and on real-world experience in addressing the cleaning, cleaning validation and microbial control challenges of regulated industries. this seminar will provide industry examples and real-world insights into development of robust cleaning programs, and will provide both a review of relevant regulatory guidance as well as practical information on validation of robust cleaning programs. the focus of this seminar will be processing equipment cleaning and cleaning validation.

seminar to be delivered in english

rouging in pharmaceutical and biopharmaceutical manufacturing systems
6/13/2012
june 25, 2012 webinar
12 pm - 1:30 pm edt (new york time)

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. there are several factors that can contribute to rouge formation including presence of halides, oxidizing chemistries, extreme ph's, high temperatures, dissimilar metallurgy or defects, improper welding, and inadequate passivation. this presentation will be divided into two parts: part i will cover the different types of rouge, its formation, and industry practices for derouging and passivating stainless steel, this part will also provide some laboratory generated data (including xps and cr/fe) demonstrating the characteristics and performance of derouging solutions. part ii will focus on presenting case studies including recommendations and procedures at different facilities.

basic concepts in cleaning and cleaning validation for gmp regulated industries
6/12/2012

steris corporation (www.sterislifesciences.com) is the industry leader in providing cleaning, cleaning validation and microbial control solutions to the pharmaceutical manufacturing industry. for over 20 years our team of experts has provided non-commercial seminars and presentations based on both current good manufacturing practices and on real-world experience in addressing the cleaning, cleaning validation and microbial control challenges of regulated industries. this seminar will provide industry examples and real-world insights into development of robust cleaning programs, and will provide both a review of relevant regulatory guidance as well as practical information on validation of robust cleaning programs. the focus of this seminar will be processing equipment cleaning and cleaning validation.

seminar to be delivered in english with simultaneous portuguese translation

effective cleaning validation practices and critical cleaning processes
5/24/2012

international pharmaceutical academy will be holding a two day course with workshops covering in detail the elements of a cleaning validation program from beginning to end. steris life sciences’ mr. michael gietl, technical service specialist and mr. paul lopolito, formulated chemistries will be speaking. *this event is no longer accepting registration*

steris life sciences group introduces the new vhp ar1200 room biodecontamination aeration unit
4/17/2012

mentor, oh, april 17, 2012: steris life sciences group introduces the new vhp ar1200 room biodecontamination aeration unit, the latest addition to its product portfolio of vaporized hydrogen peroxide (vhp) biodecontamination solutions.

steris life sciences group introduces the new vhp® victory™ room biodecontamination unit
4/10/2012

the steris life sciences group announces the addition of the new vhp victory room biodecontamination unit to its portfolio of vaporized hydrogen peroxide (vhp) biodecontamination solutions.

steris life sciences celebrates 80 years of commitment to innovation and quality in sterilization
4/2/2012

mentor, oh, -april 2, 2012: steris life sciences group’s finn-aqua® brand is celebrating 80 years of commitment to innovation and quality in sterilization. reflecting the 80 years of applied ingenuity, steris announces the release of tf-model pure steam generators and multiple-effect water stills.

designing critical cleaning processes to mitigate microbial risk in multiproduct facilities
3/29/2012

paul lopolito, technical services manager, steris corporation will be presenting at interphex 2012

“designing critical cleaning processes to mitigate microbial risk in multiproduct facilities”

online toc monitoring in gmp parts washers
3/29/2012

marcel dion, director of marketing, washing and sterilization systems, steris and george verghese, director of technical services steris to present at interphex 2012

"on-line toc monitoring in gmp parts washers”

steris life sciences service earns world class net promoter score
3/27/2012

steris life sciences group announces that its global services group has earned a net promoter score of +70, placing it among the highest rated companies in customer satisfaction.