ASP Media
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ASP is By Your Side
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Playlist
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ASP is By Your Side1
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ASP is By Your Side
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Introducing the New www.ASPJJ.com - How to Navigate the New Site1
Discover the new ASP website. We have made it...
Introducing the New www.ASPJJ.com - How to Navigate the New Site
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Discover the new ASP website. We have made it easier to find infection prevention
solutions and services that work for you.
With an interactive menu complete with images, it’s simple to find the right ASP product.
Choose the categories you’re interested in and browse relevant topics and events.
Register for ASP online education, events and webinars.
Find the right team for all your service needs.
Discover our professional education section. Current customers can access exclusive
continuing education courses!
Find the right person and department to contact, and locate your personal sales rep.
Join today at www.aspjj.com/us -
Introducing: The Redesigned STERRAD® Sterility Guide that’s SMART!1
Introducing the new STERRAD® Sterility Guide...
Introducing: The Redesigned STERRAD® Sterility Guide that’s SMART!
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Introducing the new STERRAD® Sterility Guide (SSG) with new features that make
searching for a device listing easier than ever before. The SSG is still the one source for
the most accurate and up-to-date information, as device listings are only added with the
approval of the device manufacturer. Best of all, it is still easy to use and understand.
Why is the new SSG SMART?
• SMART design to provide the optimum viewing experience across a wide range of
devices; from a computer, to tablet, to a mobile phone!
• SMART display of sterility status for all STERRAD® Systems on one page!
• SMART search tool automatically lists suggestions as you type
• SMART saving to My Inventory bookmarks the most commonly used devices
• SMART access means no more serial numbers! Register, and then log on with a
user name and password -
Introducing the new www.ASPJJ.com - Redesigned with you in mind. Discover the new ASP advantage.1
Discover the new ASP website. We have made it...
Introducing the new www.ASPJJ.com - Redesigned with you in mind. Discover the new ASP advantage.
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Discover the new ASP website. We have made it easier to find infection prevention solutions and services that work for you.
With an interactive menu complete with images, it’s simple to find the right ASP product.
Choose the categories you’re interested in and browse relevant topics and events.
Register for ASP online continuing education, events and webinars.
Now use the search bar to find the right team for all your service needs.
Register today! -
Booster Training Video1
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Booster Training Video
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ASP Public Health Message - We can do more against HAIs!1
First-of-its-kind Public Health Message (PHM)...
ASP Public Health Message - We can do more against HAIs!
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First-of-its-kind Public Health Message (PHM) featuring infection prevention experts from around the globe discussing prevention of HAIs.
The video encourages patients and healthcare professionals to join ASP in the fight against HAIs with the ultimate goal of protecting lives against infection.
DISCLAIMER: Participants in the video were not paid and were not scripted. -
Your Best Defense Against Infections - Advanced Sterilization Products1
ASP is leading the fight against healthcare a...
Your Best Defense Against Infections - Advanced Sterilization Products
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ASP is leading the fight against healthcare associated infections where they originate — from medical devices, the facility environment and human-to-human contact.
As the company behind trusted brands like STERRAD® as well as innovations like the EVOTECH® ECR and GLOSAIR™ Systems, ASP is raising the standards of infection prevention around the world — creating the safest possible environments for patients and their families, providers and communities.
Visit www.aspjj.com to learn more. -
ASP Hot Topic Webisode: Drying Medical Devices Prior to Sterilization1
Many healthcare professionals have questions ...
ASP Hot Topic Webisode: Drying Medical Devices Prior to Sterilization
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Many healthcare professionals have questions about the process of drying medical devices prior to terminal
sterilization and why it is so important.
In this Webisode you will get some insight from a clinicalperspective with an overview of standards for drying.
You can view and share this quick video segment today! -
What You Need to Know About The Updated SGNA Guidelines - Webisode 51
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What You Need to Know About The Updated SGNA Guidelines - Webisode 5
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What You Might Not Know about Meeting High-Level Disinfection Training Guidelines.1
Barbara Trattler, RN, MPA, CNOR, NE-BC Direc...
What You Might Not Know about Meeting High-Level Disinfection Training Guidelines.
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Barbara Trattler, RN, MPA, CNOR, NE-BC Director, Clinical Education
(Barbara, dressed in professional attire and either seated or standing).
Hello, I’m Barbara Trattler, Director of Clinical Education for ASP. Welcome to this edition of the ASP Hot Topic Webisode series. In this installment, we’ll address some commonly-asked questions by our customers: How do I train my staff to meet guidelines requirements for high-level disinfection...more specifically, CIDEX OPA Solutions? What tools are available to help ensure this?
These issues are hot topics for healthcare facilities and our customers, as many of you have been asked these questions by the Joint Commission on Accreditation of Healthcare Organizations (JCAHO) surveyors. In order to address them, we’ll look closely at what the guidelines say.
(Transition to Patti, dressed in professional attire)
Thank you, Barbara. Hi, I’m Patti Fritz, Senior Clinical Education Consultant for ASP. I’m going to share with you some key reasons why association guidelines say it’s important to train your staff prior to using any high-level disinfectant. Most importantly, all staff should follow manufacturer’s Instructions For Use (IFU). Later on, we are going to share some tools available from ASP to simplify training and education of your staff in order to help you follow these guidelines.
First, let’s look at the Multisociety Guideline from the American Society for Gastrointestinal Endoscopy (ASGE). It states, “Improper use of high-level disinfectants can pose safety hazards to both patients and instrument reprocessing staff. In addition, Guideline 31 says: “All personnel using chemicals should be educated about the biological and chemical hazards present while performing procedures that use disinfectants.”
How often should you evaluate your staff’s competency?
ASGE Guideline 30 says: “Competency testing of personnel that reprocess endoscopes should be performed and documented on a regular basis (e.g., at the start of use, annually). Temporary personnel should not be allowed to reprocess endoscopes until competency has been established.”
This stresses the importance of having your staff be properly trained before they begin using high-level disinfects. It is necessary to perform regular competency testing to ensure proper procedure is being followed at all times.
So, how important is staff training for those that are testing these solutions?
The Joint Standard from the American National Standards Institute (ANSI) and the Association for the Advancement of Medical Instrumentation (AAMI) note that staff who are responsible for using chemical monitors and test strips should be fully trained.
Lastly, we’ll explore the Society of Gastroenterology Nurses and Associates, or SGNA’s, standard.
The SGNA’s “Standards of Infection Control in Reprocessing of Flexible Gastrointestinal Endoscopes” says, “Ensuring your staff is properly trained is also a key component in the fight against healthcare-associated infections (HAIs), as failure to follow proper reprocessing protocol can lead to the survival of
microorganisms and an increased risk of infection.”
That is why it is so important to work with a manufacturer that provides tools and resources to support the training of your staff. At ASP, we have a number of tools to help make the process of training your staff as smooth and easy as possible.
(Show In-Service Kit…inside of the binder and highlight the CD. )
For example, ASP provides an In-Service Kit for CIDEX® OPA Solutions which includes materials designed to be your resource in training your staff on on-going basis. The Kit includes everything you need to properly use and test CIDEX® OPA Solution for high-level disinfection, including a CD that provides education and instructions in a convenient binder.
This in-service kit can help address many of the common questions that we hear from our customers. For example, many of you have asked about what types of materials and medical devices can be used with CIDEX® OPA Solution (Show tab 3 to show the Technical Information). The Technical Information included in the In-Service Kit lists all materials that CIDEX® OPA Solution has been tested for, including a variety of metals, plastics, elastomers and adhesives.
(Show the log book). Customers are also curious about how to use CIDEX® Test Strips. These are used to ensure the minimum effective concentration (MEC) required for high-level disinfection, and it is recommended that you test CIDEX® OPA Solution prior to each usage. To help with this process, the kit also includes a data sheet and IFU for CIDEX® OPA Solution Test Strips, as well as a log book to record your test results (Show a log sheet within the log book). On this sheet you can record your quality controls, temperature reads and test results. -
Additional Information For Transitioning from the STERIS System 11
In this Webisode, we will look to discuss the...
Additional Information For Transitioning from the STERIS System 1
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In this Webisode, we will look to discuss the December 22 announcement by FDA regarding the extended support period for customers who have already purchased a legally marketed alternative to the Steris System 1 reprocessor.
For healthcare facilities that have yet to acquire a replacement product for their current SS1 units, they will need to issue a purchase order for that product by February 2, 2012. Only customers who have placed orders for an alternative solution and completed a "Certificate of Transition" may continue receiving support from STERIS through August 2, 2012.
By now you have probably received a letter from STERIS dated December 22 requesting that if you intend to continue purchasing S20 sterilant to do the following:
1. Purchase a legally marketed alternative
2. Complete and sign the STERIS "Certificate of Transition"
3. Return the "Certificate of Transition" to STERIS Corporation
We recommend that you complete these steps as soon as possible to ensure continuity in reprocessing instruments for your patients. STERIS will discontinue support for SS1 customers who do not provide them a completed "Certificate of Transition".
Although the FDA announcement does not change your timeframe for purchasing a replacement product for your SS1s, the announcement does provide you with additional time to properly implement an alternative solution within your facility and minimize impact to your patient flow.
The position of ASP has not changed due to the December 22 FDA announcement. Since FDA issued the Steris System 1 safety alert over two years ago, we have remained committed to delivering alternative solutions in a timely manner and raising the standard of care.
You can be confident that orders placed for ASP terminal sterilization or high-level disinfection systems by February 2, 2012 will be delivered, installed, and in-serviced in advance of the August 2, 2012 deadline by FDA.
For those who are still evaluating your options, keep in mind that not all alternatives out there are recommended for processing critical devices.
For example, the newly released Steris System 1E™ liquid chemical sterilant processing system is not a sterilizer.
According to FDA, "sterilization with liquid chemical sterilants does not convey the same sterility assurance as sterilization using thermal or gas/vapor/plasma low temperature sterilization methods."
Our STERRAD® Sterilization Systems provide you the sterility assurance level you need for your critical devices, and the STERRAD® CYCLESURE® 24 Biological Indicator provides you the peace of mind that proper sterilization conditions were achieved.
Thousands of facilities in the US turn to STERRAD® Sterilization Systems to keep up with their surgical demand and provide their patients with instruments that have been processed using the highest standard of care, terminal sterilization.
The STERRAD® NX® System, with its ability to quickly sterilize a wide range of surgical instruments from cameras to single-channel flexible scopes makes it possible to safely achieve sterilization in the operating room (OR).
If you are looking to replace your SS1 in the GI or Respiratory setting, our EVOTECH® Endoscope Cleaner and Reprocessor (ECR) is the first endoscope reprocessor that can eliminate the need to manually clean your scopes before reprocessing.
This cutting edge product removes the variability in human factors associated with cleaning endoscopes, properly documenting and monitoring of minimally effective concentration (MEC) of your disinfection solution.
We at ASP understand that managing this change can be challenging and are committed to helping you start this process as soon as possible.
In the last two years, we have helped thousands of facilities transition to our STERRAD® Systems and EVOTECH® ECRs.
Our highly experienced clinical education team, top notch field service engineers and tenured sales professionals are ready to help you raise the standard of care for your patients.
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Got Laryngoscopes? Get Answers with the ASP Hot Topic Webisodes!1
in this Webisode, we will look at the issue o...
Got Laryngoscopes? Get Answers with the ASP Hot Topic Webisodes!
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in this Webisode, we will look at the issue of what to do with anesthesia laryngoscope blades when it comes to reprocessing them. We will give an overview of the new standards issued by the Joint Commission and then discuss practical solutions, based on the application of the standards.
First, the CDC’s Healthcare Infection Control Practices Advisory Committee known as (HICPAC) classifies laryngoscope blades as “semicritical” items. “Semicritical” items are defined as “items that directly or indirectly contact mucous membranes of the respiratory tract. They should be sterilized or subjected to high-level disinfection before reuse.”
On October 24, 2011, The Joint Commission issued a new standards-related FAQ addressing the processing and storing of laryngoscope blades in perioperative-care settings, and following on November 3, AORN informed its members of the new standards-related FAQ.
What did the FAQ say and what does it mean for you? The FAQ emphasizes that Joint Commission surveyors will evaluate processes related to laryngoscope blades to ensure that they are safe for use on the next patient. This will include checking that laryngoscope blades are processed properly, either with sterilization or with high-level disinfection, and packaged and stored in such a way that would prevent recontamination.
The FAQ stated that the CDC’s 2008 Disinfection & Sterilization Guideline does not address the issue of packaging, however an earlier standard does have a specific recommendation which states that appropriate rinsing, drying and packaging is strongly recommended and supported by well-designed experimental, clinical or epidemiologic studies.
While appropriate packaging is recommended, it is important to note that HICPAC guidelines do not specify the manner in which laryngoscope blades should be packaged, only that the packaging prevent recontamination.
According to the Joint Commission, compliant methods of storage include, but are not limited to: a peel pack post-steam sterilization for long-term, or wrapping in a sterile towel for short-term. Noncompliant methods include storing unwrapped blades in an anesthesia drawer or on top of a code cart.
Because laryngoscope handles are considered contaminated after use, they must also be processed prior to use on the next patient. Many manufacturers suggest a low-level surface disinfectant be utilized on the surface of the handle, but check your manufacturer’s indications for use (IFU) as processes vary by manufacturer. In addition, some state laws require additional processing, so check your state for any additional applicable laws or regulations.
Okay, now that we have looked at the new standards and guidance from the Joint Commission, let’s talk about practical solutions and best practices to the proper reprocessing, packaging and storage of your laryngoscope blades.
From our perspective the best option for reprocessing your laryngoscope blades is through terminal sterilization, such as STERRAD® Technology, where you can use a peel pack for visibility.
In addition, reprocessing should always be done in the sterile processing department or operating room/sub-sterile core. It’s also a good practice to make sure your staff is educated on processing reusable medical devices, including those outside the sterile processing department, such as nurses and physicians.
An alternate option is to process the blades using high-level disinfectant and rinse with demineralized water. Then dry the devices completely, package securely and store until they are ready for use.
Additionally, remember to disinfect or sterilize battery handles and always clean the battery charger stands, as it can be exposed to dust and bacteria. It is not recommended to store blades for the long term (states in previous page can store for short term in sterile towel) in absorbable materials, such as towels. Also, remember not to store blades wet in a sealed pouch or container.
The STERRAD® Systems from ASP help you address changing standards like this one and be more prepared to pass Joint Commission surveys. All of ASP’s STERRAD® Systems are equipped to terminally sterilize laryngoscope blades using a peel pack for visibility. As always, please reference the device manufacturers’ IFU for processing instructions.
ASP STERRAD® Systems are approved to process a number of other reusable medical devices, such as
fiberoptic laryngoscopes, optical stylets, flexible intubation endoscopes and video intubation endoscopes.
As a STERRAD® Systems customer, you can conveniently check the STERRAD® Sterility Guide (or SSG), a frequently updated, easy-to-use online tool designed to help you identify which devices fall within STERRAD® Systems cleared claims for sterility. The guide can be accessed on your computer or smartphone at www.sterradsterilityguide.com. For more information on dev ices cleared for reprocessing in STERRAD® Systems, please contact the Medical Device Manufacturer’s Program at ASP at mdmprogram@its.jnj.com .
AD-12005-01-US_A -
How Am I Supposed to Clean and Sterilize My Devices?1
In this Webisode we will address one of the m...
How Am I Supposed to Clean and Sterilize My Devices?
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In this Webisode we will address one of the most common questions asked by our customers today. “What information should I follow to determine approved cleaning and sterilization instructions?”
This issue of IFU compliance is a hot topic and area of focus for many healthcare facilities right now, and we are going to explore this subject today, looking closely at what the AAMI standards have to say. In addition we’ll also discuss some practical options for you and your facility.
First, let’s look at the amendment to AAMI standard ST79 for sterilization. In section 7.2.2 it states:
“The written IFU of the device manufacturer should always be followed. The reusable medical device manufacturer is responsible for ensuring that the device can be effectively cleaned and sterilized…The manufacturer’s written IFU should be kept on file and periodically reviewed for any updates. If there are no specific written IFU instructions in the labeling, then the manufacturer should be contacted directly to provide a documented method.” 1
AORN also supports AAMI ST79 and state in their AORN Recommended Practices for Cleaning and Care of Surgical Instruments and Powered Equipment that “The manufacturer’s written, validated instructions for handling and reprocessing should be obtained and evaluated to determine the ability to ade¬quately clean and reprocess the equipment within the health care facility before purchasing surgical instruments and powered equipment.” 2
Because the Joint Commission and other agencies want to make sure you are following the most updated standards and instructions, it has become the facility’s responsibility to comply with the latest IFUs. Medical device manufacturers, or MDMs, are continually updating IFUs to meet regulatory guidelines; so even an IFU that is only two to three years old may already be out of date.
How can you streamline this process of being up to date with IFUs?
In this dynamic environment and increasing focus on IFU compliance we are pleased to report that STERRAD® Systems are currently listed in IFUs by many device manufacturers for terminal sterilization. At ASP, we work closely with many Medical device companies to make sure we maintain the most current IFUs for instruments listed in our online reference tool, the STERRAD® Sterility Guide, also known as the SSG. Every device listed in the SSG is backed by an acknowledgment from the device manufacturer in their labeling or instructions for use.
It’s worth noting that we are constantly adding new devices to the SSG. In fact in the last two months alone, we added thousands oflistings. As a general purpose sterilizer, STERRAD® Systems can process many stainless steel accessories and instruments, as well as the critical devices listed on the SSG.
Visit SSG http://www.sterradsterilityguide.com/.
Or for more information, visit ASP at http://www.aspjj.com.
AD-120105-01-US_A -
25th Anniversary History Video (External Version)1
...
25th Anniversary History Video (External Version)
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Learn More. Make an Impact. AORN 2012 Video1
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Learn More. Make an Impact. AORN 2012 Video
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Privacy Policy
Privacy Policy
Last Updated: August 2013
Advanced Sterilization Products, Division of Ethicon US, LLC. is concerned about privacy issues and wants you to be familiar with how we collect, use, and disclose information. This Privacy Policy describes our practices in connection with information that we or our service providers collect through the Web site or Web property (including, for example, a mobile Web site or application) operated and controlled by us from which you are accessing this Privacy Policy (each, the “Site”). By providing personal information to us or by using the Site, you agree to the terms and conditions of this Privacy Policy.
INFORMATION COLLECTION
Information You Provide
Some areas of the Site may ask you to submit personal information in order for you to benefit from the specified features (such as newsletter subscriptions, tips/pointers, or order processing) or to participate in a particular activity (such as sweepstakes or other promotions). You will be informed what information is required and what information is optional.
We may combine the information you submit with other information we have collected from you, whether on- or offline, including, for example, your purchase history. We may also combine it with information we receive about you from other sources, such as other Johnson & Johnson Operating Companies, publicly available information sources (including information from your publicly available social media profiles), and other third parties.
Passive Information Collection and Use
As you navigate around the Site, certain information can be passively collected (that is, gathered without your actively providing the information), using various technologies. We and our third party service providers passively collect and use information in a variety of ways, including:
Through your browser: Certain information is collected by most browsers, such as your Media Access Control (MAC) address, computer type (Windows or Macintosh), screen resolution, operating system version, and Internet browser type and version. We may collect similar information, such as your device type and identifier, if you access the Site through a mobile device.
Using cookies: Cookies are pieces of information stored directly on the computer you are using. Cookies allow us to collect information such as browser type, time spent on the Site, pages visited, and language preferences. We and our service providers use the information for security purposes, to facilitate navigation, display information more effectively, and to personalize your experience while using the Site. We also use cookies to recognize your computer or device, which makes your use of the Site easier, such as to remember what is in your shopping cart. In addition, we use cookies to gather statistical information about Site usage in order to continually improve its design and functionality, understand how individuals use it, and to assist us with resolving questions regarding it. Cookies further allow us to select which of our advertisements or offers are most likely to appeal to you and display them while you are on the Site. We may also use cookies in online advertising to track consumer responses to our advertisements.
You can refuse to accept these cookies by following your browser’s instructions; however, if you do not accept them, you may experience some inconvenience in your use of the Site. You may also not receive advertising or other offers from us that are relevant to your interests and needs. To learn more about cookies, please visit http://www.allaboutcookies.org.
Using Flash cookies: Our use of Adobe Flash technology (including Flash Local Stored Objects (“Flash LSOs”)) allows us to, among other things, serve you with more tailored information, facilitate your ongoing access to and use of the Site, and collect and store information about your use of the Site. If you do not want Flash LSOs stored on your computer, you can adjust the settings of your Flash player to block Flash LSO storage using the tools contained in the Website Storage Settings Panel. You can also control Flash LSOs by going to the Global Storage Settings Panel and following the instructions (which may include instructions that explain, for example, how to delete existing Flash LSOs (referred to as “information” on the Macromedia site), how to prevent Flash LSOs from being placed on your computer without your being asked, and (for Flash Player 8 and later) how to block Flash LSOs that are not being delivered by the operator of the page you are on at the time). Please note that setting the Flash Player to restrict or limit acceptance of Flash LSOs may reduce or impede the functionality of some Flash applications, including, potentially, Flash applications used in connection with the Site or our online content.
Using pixel tags, web beacons, clear GIFs, or other similar technologies: These may be used in connection with some Site pages and HTML-formatted e-mail messages to, among other things, track the actions of Site users and e-mail recipients, measure the success of our marketing campaigns, and compile statistics about Site usage and response rates.
Online behavioral advertising: The use of cookies, pixel tags, web beacons, clear GIFs, or other similar technologies allows our third-party vendors to deliver advertisements about our products and services when you visit the Site or other web sites or web properties across the Internet. These vendors may place pixel tags, web beacons, clear GIFs, or similar technologies on the Site and other websites or web properties, and also place or recognize third-party cookies when you visit the Site or other sites or web properties. They may use information about your visits to the Site and other web sites or web properties to provide advertisements about goods and services that may be of interest to you.
IP Address: Your IP Address is a number that is automatically assigned to the computer that you are using by your Internet Service Provider. An IP Address is identified and logged automatically in our server log files whenever a user visits the Site, along with the time of the visit and the page(s) that were visited. Collecting IP Addresses is standard practice on the Internet and is done automatically by many web sites. We use IP Addresses for purposes such as calculating Site usage levels, helping diagnose server problems, and administering the Site.
How We Use and Disclose Information
We use and disclose information you provide to us as described to you at the point of collection.
We also use information from or about you:
- to respond to your inquiries and fulfill your requests, such as to send you documents you request or e-mail alerts;
- to send you important information regarding our relationship with you or regarding the Site, changes to our terms, conditions, and policies and/or other administrative information; and
- for our business purposes, such as data analysis, audits, developing new products, enhancing our website, improving our products and services, identifying Site usage trends, personalizing your experience on the Site by presenting products and offers tailored to you, and determining the effectiveness of our promotional campaigns.
We also disclose information collected through the Site:
- to our affiliates for the purposes described in this Privacy Policy. A list of our affiliates is available here (click on the link for Form 10K, Exhibit 21, under “SEC Filings”). Advanced Sterilization Products, a division of Ethicon US, LLC. is the party responsible for the management of the jointly-used Personal Information;
- to our third party partners with whom we offer a co-branded or co-marketed promotion;
- to our third party service providers who provide services such as website hosting and moderating, mobile application hosting, data analysis, payment processing, order fulfillment, infrastructure provision, IT services, customer service, e-mail and direct mail delivery services, credit card processing, auditing services, and other services, in order to enable them to provide services; and
- to a third party in the event of any reorganization, merger, sale, joint venture, assignment, transfer, or other disposition of all or any portion of our business, assets, or stock (including in connection with any bankruptcy or similar proceedings).
In addition, we use and disclose information collected through the Site as we believe to be necessary or appropriate: (a) as permitted by applicable law, including laws outside your country of residence; (b) to comply with legal process; (c) to respond to requests from public and government authorities, including public and government authorities outside your country of residence; (d) to enforce our terms and conditions; (e) to protect our operations or those of any of our affiliates; (f) to protect our rights, privacy, safety, or property, and/or that of our affiliates, you, or others; and (g) to allow us to pursue available remedies or limit the damages that we may sustain. We may also use and disclose information collected through the Site in other ways, with your consent.
We also use and disclose information we collect passively as described above, under “Passive Information Collection and Use,” and for any other purpose, except where we are required to do otherwise under applicable law (for example, if we are required to treat such information as personal information). In addition, we may use and disclose information that is not in personally identifiable form for any purpose. If we combine information that is not in personally identifiable form with information that is (such as combining your name with your geographical location), we will treat the combined information as personal information as long as it is combined.
THIRD PARTY SITES AND SERVICES
This Privacy Policy does not address, and we are not responsible for, the privacy, information, or other practices of any third parties, including any third party operating any site or web property (including, without limitation, any application) that is available through this Site or to which this Site contains a link. The availability of, or inclusion of a link to, any such site or property on the Site does not imply endorsement of it by us or by our affiliates.
SECURITY
We use reasonable organizational, technical, and administrative measures to protect personal information under our control. Unfortunately, no data transmission over the Internet or data storage system can be guaranteed to be 100% secure. If you have reason to believe that your interaction with us is no longer secure (for example, if you feel that the security of any account you have with us has been compromised), please immediately notify us of the problem by contacting us in accordance with the Contacting Us section below.
CHOICES AND ACCESS
Your choices regarding our use and disclosure of your personal information
We give you choices regarding our use and disclosure of your personal information for marketing purposes. You may opt out from:
- Receiving marketing communications from us: If you no longer want to receive marketing communications from us on a going-forward basis, you may opt out of receiving them by contacting us via e-mail to contactASP@its.jnj.com. In your response to us, please provide your name, identify the form(s) of marketing communications that you no longer wish to receive, and include the address(es) to which it/they are sent]. For example, if you no longer wish to receive marketing e-mails or direct mail from us, tell us that, and provide your name and e-mail or postal address. You may also opt out of receiving marketing communications from us by visiting the Site to update your online profile. In addition, you may opt out of receiving marketing e-mails from us by following the unsubscribe instructions provided in any such message.
- Our sharing of your personal information with affiliates and third-party partners: If you would prefer that we not share your personal information on a going-forward basis with our affiliates and/or third-party partners for their marketing purposes, you may opt out of this sharing by contacting us by e-mail to contactASP@its.jnj.com. In your response to us, please state that we should no longer share your personal information with our affiliates and/or third-party partners for their marketing purposes, and include your name and e-mail address.
We will seek to comply with your request(s) as soon as reasonably practicable. Please note that if you opt out as described above, we will not be able to remove your personal information from the databases of our affiliates with which we have already shared your information (i.e., as of the date that we implement your opt-out request). Please also note that if you opt out of receiving marketing-related messages from us, we may still send you important transactional and administrative messages, from which you cannot opt out.
How you can access, change, or delete your personal information
If you would like to review, correct, update, or delete the personal information that you have provided via the Site, please contact us via e-mail to contactASP@its.jnj.com. We will try to comply with your request as soon as reasonably practicable. You may also visit the Site to update your online profile.
RETENTION PERIOD
We retain your personal information for the period necessary to fulfill the purposes outlined in this Privacy Policy, unless a longer retention period is required or allowed by law or to otherwise fulfill a legal obligation.
USE OF SITE BY MINORS
The Site is not directed to individuals under the age of 13, and we request that these individuals not provide Personal Information through the Site.
CROSS-BORDER TRANSFER
Your personal information may be stored and processed in any country where we have facilities or service providers, and by using our Site or by providing consent to us (where required by law), you agree to the transfer of information to countries outside of your country of residence, including to the United States, which may provide for different data protection rules than in your country.
SENSITIVE INFORMATION
Unless we specifically request or invite it, we ask that you not send us, and you not disclose, any sensitive personal information (e.g., information related to racial or ethnic origin, political opinions, religion or other beliefs, health, criminal background or trade union membership) on or through the Site or otherwise to us. In those cases where we may request or invite you to provide sensitive information, we will do so with your express consent.
UPDATES TO THIS PRIVACY POLICY
We may change this Privacy Policy. Please take a look at the “LAST UPDATED” legend at the top of this page to see when this Privacy Policy was last revised. Any changes to this Privacy Policy will become effective when we post the revised Privacy Policy on the Site. Your use of the Site following these changes means that you accept the revised Privacy Policy.
CONTACTING US
If you have any questions about this Privacy Policy, please contact us by e-mail at contactASP@its.jnj.com., or please write to the following address:
Advanced Sterilization Products
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