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Secteurs d’activité

  • Fabrication de produits pharmaceutiques

    Solutions personnalisées destinées aux fabricants de principes actifs pharmaceutiques(PAP) ou de produits pharmaceutiques finis, par exemple comprimés, capsules, doses liquides et médicaments parentéraux.

  • Biotechnologie

    Solutions personnalisées pour l’élaboration et le remplissage de médicaments, de vaccins et de traitements dans diverses posologies, en production de petits lots ou en masse.

  • Recherche et laboratoire

    Solutions personnalisées destinées au contrôle des contaminations dans le cadre des recherches impliquant des rongeurs, des petits animaux et des primates afin de pouvoir commercialiser les résultats au plus tôt.

  • Dispositifs médicaux

    Solutions personnalisées destinées à la désinfection ou à la stérilisation des dispositifs homologués par les autorités sanitaires américaines (FDA) de classe 1, classe 2 ou classe 3, des joints implantables aux poches d’intraveineuse stérilisées.

  • Cosmétique

    Solutions personnalisées aidant à maintenir un environnement propre et contrôlé pendant la fabrication de produits cosmétiques.

  • Compléments alimentaires

    Solutions personnalisées destinées au contrôle des contaminations pendant la fabrication de compléments alimentaires de haute qualité afin de garantir la sécurité des produits.

Recent News

steris life sciences webinar - gmp vs non-gmp washers and sterilizers
12/9/2016 3:50 PM
in our upcoming steris life sciences webinar, we will be discussing the characteristics that differentiate “gmp” from regular or “laboratory” equipment. 

steris life sciences webinar - three reasons why stainless steel maintenance is critical to your processes
11/29/2016 7:16 AM
in our upcoming steris life sciences webinar, we will be discussing three reasons why stainless steel maintenance is critical to your processes.

cleaning validation in continuous manufacturing
11/14/2016 10:12 AM

using continuous manufacturing process? our experts share a lifecycle cleaning validation approach on pharmtech.com

worst case biofilm conditions for cleaning evaluations
11/14/2016 10:23 AM

what’s the biggest influence of biofilm formations? it’s not the surface type! get our expert findings @crtmagazine

guideline to disinfectant validation webinar
11/2/2016 10:31 AM

join jim polarine, steris' technical services expert, as he covers a webinar on validation and performance testing of antimicrobial technologies.

steris life sciences webinar - nist/iso traceable calibration program webinar
11/2/2016 11:11 AM
join the steris life sciences team for a wonderful learning opportunity during our upcoming webinar focusing on a walkthrough of nist/iso traceable calibration programs.

steris life sciences webinar - automated washing: basic principles and common mistakes
11/2/2016 10:31 AM
in our upcoming steris life sciences webinar, we will be discussing automated washing, basic principles and common mistakes.

aalas 67th national meeting in charlotte, nc
10/27/2016 2:15 PM

join us at the largest gathering of professionals devoted to the care and use of laboratory animals at the 67th annual american association for laboratory animal science (aalas) national meeting. 

pack expo international & pharma expo 2016
10/27/2016 2:31 PM
planning to attend the pack expo international & pharma expo 2016 in chicago? don’t miss our presentation, cleaning validation concerns for continuous manufacturing processes on november 8 at 1 pm.
validation and requalification of steam sterilizers webinar
10/27/2016 2:47 PM
join us for a free webinar on tuesday, november 1st from 10:00 a.m. to 11:30 a.m. edt. 
steris corporation launches the reliance® 300xls laboratory glassware washer
9/19/2016 9:49 AM
available for order, the new washing system provides a smaller footprint and maximum productivity.
ispe signapore conference
7/27/2016 8:00 AM

steris professionals will be presenting at the ispe singapore conference, august 24 – 27.  join us!

ispe nordic cop critical utilities seminar at the steris finn-aqua tuusula facility, finland
7/22/2016 7:19 AM
join us at the steris finn-aqua manufacturing facility in tuusula, finland on september 7th for the ispe nordic cop critical utilities seminar: future technologies and high purity water.
ispe nordic cop critical utilities seminar at nne pharmaplan in denmark, high purity water and future technologies
7/22/2016 7:17 AM
join us on september 6th in denmark for the ispe nordic cop critical utilities seminar: high purity water and future technologies.
international symposium for contamination control (iscc) brazil
7/21/2016 2:26 PM
join steris at the 23rd edition of the international confederation of contamination control societies (icccs) global event in sao paulo, brazil.
designing and implementing an effective cleaning and disinfection program webinar
6/16/2016 10:25 AM

join steris experts via webinar while they cover the topic of "designing and implementing an effective cleaning and disinfection program"on june 28, 2016 at 12:00 pm edt.

steam in place sterilization webinar - design, process and validation
6/16/2016 10:43 AM

join steris experts via webinar while they provide an overview of steam-in-place sterilization, specifically regarding engineering of the system, process development, monitoring and validation expectations on june 29, 2016 at 2:30 pm edt.

pre-filled syringes west coast conference
5/25/2016 8:16 AM

steris will be exhibiting at smi's pre-filled syringes west coast conference on june 6-7, 2016 in san diego. 

biofilm remediation strategies webinar
5/5/2016 10:22 AM

join steris experts for a holistic approach to remediate biofilm contamination via webinar on may 18, 2016 at 12:00 pm edt.

cleaning and disinfection best practices for the cleanroom environment webinar
5/2/2016 8:54 AM
cleaning and disinfection best practices for the cleanroom environment webinar, may 18, 2016


designing an effective cleaning and disinfection system is a critical part of the facility operations and contamination control program to meet fda, ema and mhra regulations. join steris' industry experts aaron mertens and jim polarine on may 18 as they explain how to be compliant.

steris life sciences speaker sessions at the 2016 cleaning validation summit
4/13/2016 10:10 AM

may 23 - 24, 2016

steris life sciences technical services manager’s, beth kroeger and walid el azab, both will be presenting at the summit.  this two-day intensive summit brings together industry leaders to help you exceed regulatory thresholds and avoid costly fda inspection findings.  register your space and be sure to stop for their presentation.  


general econopak, inc. (gepco) to become steris barrier product solutions
4/4/2016 8:00 AM

steris life sciences product offerings continue to grow with the acquisition of general econopak, inc (gepco).  as part of this transition, the gepco team will be changing their name to steris barrier product solutions.  please click here for the customer notification letter and faq document for further details.   

steris and controlled contamination services to offer streamlined cleanroom sterilization and decontamination processes to customers
4/4/2016 9:00 AM

steris and controlled contamination services to offer streamlined cleanroom sterilization and decontamination processes to customers

mentor, ohio – april 4, 2016 – steris corporation and controlled contamination services (ccs) recently collaborated to offer integrated services to their life sciences customers. this relationship streamlines cleanroom sterilization and decontamination by incorporating steris’s patented vhp® biodecontamination solutions with ccs’s comprehensive cleaning program.

steris corporation launches new small research steam sterilizer
4/1/2016 7:21 AM

new sterilization system delivers a leap in energy savings and control capability

 

mentor, ohio – april 1, 2016 – the research market globally requires steam sterilizers that are easy to use, cost effective, and able to keep up with advances in control capabilities.  in response, steris is releasing the next edition to the ls series, the amsco® 110ls and 250ls small steam sterilizers.
the basics of fume hood exhaust monitoring
3/1/2016 1:00 PM

learn more from steris expert, scott alexander, an advanced certification technician with agape instruments service, in this recent article, "the basics of fume hood exhaust monitoring." featured in controlled environments february 2016 edition.

steris life sciences speaker sessions at the 2016 pda europe conference: pharmaceutical microbiology
2/15/2016 2:05 PM

join steris life sciences on february 23rd and 24th at the 2016 pda europe conference on pharmaceutical microbiology in berlin germany.  

join steris for an upcoming seminar in the bay area
1/14/2016 8:15 AM
join steris for our upcoming seminar, "contamination control strategies for addressing biofilm & bioburden.  the seminar will be held on march 3, 2016 in the bay area.  sign up here
learn more about the steris vhp lts-v in the uk at the smi conference on january 27th and 28th
12/31/2015 9:25 AM

juha mattila of steris life sciences will present at the 8th annual smi conference.  his presentation will focus on the vhp lts-v product.  learn more about the conference here

join steris for a vhp® seminar in berlin
12/22/2015 1:22 PM

join steris life sciences for an upcoming vhp® seminar in april 2016 in berlin.

contact gerhard_lauth@steris.com for details on registration. 


principes du lavages automatique et erreurs courantes
12/15/2015 10:28 AM
learn more from steris experts in this recent article, "principes du lavages automatique et erreurs courante."  featured in la vaue's 's september 2015 edition



steris life sciences upcoming webinars
12/2/2015 1:44 PM

steris life sciences upcoming webinars 


register here for, “disinfectant rotation and residue removal”
december 8th  @ 10 am et

register here for, “design considerations for effluent treatment in bio-containment facilities”
december 10th  @ 10 am et

register here for, “sterilant safe handling”
december 10th  @ 10 am et

register here for, "a walkthrough of a nist/iso traceable calibration program"

december 10th @ 10 am et

upcoming steris life sciences fall webinar series
10/27/2015 10:37 AM

steris life sciences fall webinar series 

from formulated chemistries, to capital equipment to parts & services, steris life sciences is science and solutions for life. steris invites you to join us for an upcoming webinar. we have an exciting schedule of upcoming programs with topics such as cleaning validation programs, understanding key industry regulations, green principles, and terminal sterilization.

register here for, “considerations for cleaning validation using automated washing systems”
october 29th @ 11 am et

register here for, “lab waste sterilization challenges”
november 3rd @ 10 am et

register here for, “join steris life sciences to learn more about permitted daily exposure (pde) values for residual active substances”
november 5th @ 11 am et

register here for, “vhp lts-v low temperature surfaces terminal sterilization”
november 12th @ 10 am et 


pharma expo: insights from steris expert, elizabeth rivera, on new cleaning validation strategies
10/16/2015 8:45 AM

elizabeth rivera, technical services manager at steris revealed in her presentation at pharam expo, “the process lifecycle model: a new approach to cleaning validation,” the mindset in pharmaceutical manufacturing is shifting toward an approach in which continuous monitoring plays an important role, due in part to fda guidance for process validation general principles and practices (2011). she notes this shift to continuous monitoring helps ensure effective cleaning procedures.


steris corporation launches the finn aqua 77 series medium steam sterilizer globally
10/1/2015 3:30 PM

mentor, ohio – october 1st, 2015 – steris corporation announces the addition of the finn-aqua 77 series medium steam sterilizer to its line of laboratory steam sterilization systems. this new product line is designed to help steris research customers better address their specific decontamination needs.

ispe nordic advanced aseptic processing conference in denmark, current trends and advanced technology used in aseptic processing
9/15/2015

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
9/15/2015

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
9/15/2015

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
6/17/2015
  • 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
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.

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.

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”

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”

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.

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