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New DNA-based methods for the skin microbiome

DNA-based methods for skin microbiome
DNA

We will develop and validate robust DNA-based methods (qPCR and NGS) to quantify bacteria in the skin's microbiome. The project provides the basis for studies of the skin's microbiome to study, for example, the effect on the composition when applying different skin care products.

Project leader
Active
Infection control Chemical and biological analysis Generic metrology and measurement technology
2020-2023
Division: Division Bioeconomy

It has long been known that the human body is colonized by a diversified microbiome consisting of bacteria, archaea and fungi. In addition, it is well documented that imbalances between naturally occurring microorganisms caused by, among other things, antibiotic treatment have a crucial role in several skin diseases.

In order to study the composition and change of the microbiome, there is a need for sensitive and robust methods of analysis. The use of quantitative PCR (qPCR) and large-scale sequencing (NGS) has revolutionized our understanding of the composition and richness of skin flora over the past ten years. The research on maintaining a well-functioning microbiome on our skin when using skin care products is a relatively unexplored area. There are several descriptive studies based on qPCR and NGS of the body's microbiome, but since the composition and richness of the microbiome varies significantly between different skin surfaces, it is not possible to draw general conclusions about the microbiome's influence on a particular product or substance.

Although the skin contains a large number of microorganisms, the presence of an excess of human DNA makes it difficult to apply DNA-based methodology, this is especially true of NGS. Some DNA-based methods are also sensitive to the presence of disruptive substances in the samples, e.g. from skin care products applied to the skin. These challenges mean that optimization work is necessary to get well-functioning and robust methods. Standardized methods for this purpose are often missing.

Charlotta Löfström

Senior Forskare
+46 10 516 67 30 Read more about Charlotta
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3. Good health and well-being
12. Responsible consumption and production
Project end date: Infection control Sekundär områdes navigation:
Metrology
Biotechnology
Food
Chemical and biological analysis

ISO 17664 Validating Instruction for Users for cleaning and disinfection

Name of service (page headline, shown in promos – maximum of 70 characters incl. spaces): ISO 17664 Validating Instruction for Users - cleaning and disinfection Lead (include SEO-words and the main benefits for your target groups. Stick to one paragraph, maximum 2-3 sentences):

For reusable medical devices, there must be a validated Instruction for Users (IFU) for cleaning and disinfection. We assist in creating a functional instruction according to both ISO 17664-1 and ISO 17664-2 and validate that the products are properly cleaned and disinfected.

Purpose/Benefit:

It is crucial to follow ISO 17664-1 and ISO 17664-2 as these standards ensure that medical devices are handled in a way that minimizes the risk of infections. Proper cleaning and disinfection are essential to prevent the transmission of harmful bacteria to patients.

By adhering to these standards, manufacturers and healthcare providers can guarantee that products are safe to use and meet regulatory requirements, such as those outlined in the MDR.

This strengthens trust in the quality and reliability of the products, while contributing to enhanced patient safety.

Method (what/which methods are used to perform the service):

The cleaning procedure is validated by soiling the product with appropriate contaminants, such as blood or artificial soil, followed by cleaning and analysis of any remaining soil residues through methods such as protein analysis or hemoglobin analysis, according to ISO 15883-5 (MDR) or ANSI/AAMI ST98 (FDA).

We can also evaluate automatic (thermal) disinfection with temperature probes to ensure that the product meets the expected A0 value, according to ISO 15883-1 (MDR). Manual (chemical) disinfection processes are validated according to ANSI/AAMI TIR12 (FDA).

Delivery (what does the client get after performed service – e.g. a report, certificate etc.):

Methods and results are presented in a written report, in Swedish or English.

Area:
Infection control
Chemical and biological analysis
Medical devices
Contact person (Enter one name per field. Activated personal contact pages will appear automatically): Louise Wogelred, Forsknings- och utvecklingsingenjör
Medical Devices – validation of cleaning and disinfection
Field measurements: No Price type: 1 Division: Division Materials and Industry Preparation: Description of preparation Certification and marking: Not applicable Type of service: Not applicable Instrument: Not applicable General area: Not applicable Order information: Please find contact information below Divison (OLD): Division Materials and Industry Delivery level: Non-accredited
louise.wogelred@ri.se,
/en/personal-data-processing/candidate-database
More information:

At RISE, we are pleased to offer services that ensure your products can be cleaned, disinfected, and sterilized safely and effectively according to ISO 17664-1/2, ISO 15883-5, ANSI/AAMI ST98, and ISO 17665:2024. We also provide testing services for evaluating the biocompatibility of medical devices according to ISO 10993-5:2009 and ISO 10993-23:2021.

By combining our services under these standards, we can help you ensure that your medical devices are biocompatible, sterile, and suitable for reuse—critical factors for patient safety and product success in the market.

Please feel free to contact me for a consultation.

3. Good health and well-being
Purpose - Header: Safe products, safe patients Metod - Header: Method
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Medtech Sekundär områdes navigation:
Metrology
Infection control
Tjänstetyp tagg: Verifiering och validering

Cleaning and disinfection

Cleaning and disinfection

Is it not as clean as it should? Which chemicals or materials are the best? How do you measure cleanliness? How can one resource optimise its cleaning process?

Does your company have a product or a new idea linked to hygiene, cleaning and disinfection, but need help to further develop or test it?  Does your company need to optimise cleaning and disinfection? Is it really clean but with a lower environmental footprint? These are some of the questions we can help answer.

 offers independent evaluation and development of product/technology/materials/routines/services regarding both hygiene improvements and functional properties in lab, pilot or full scale

We offer, among other things, the following services:

  • Cleanability of Process Equipment
  • Formulation & Evaluation of cleaning agents
  • Comparison of cleaning techniques
  • Numerical Purity Analysis
  • Just as clean – but with a lower environmental footprint
  • Efficient Use of resources 
  • Safe working environment 
  • Investigation of cleaning problems
  • Medical devices – cleaning, sterilization validation
  • Biofilm 
  • Hygienic Design 
  • Training 

 

Lina Lindahl

Forskare
+46 10 516 56 86 Read more about Lina
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Lars Hamberg

Senior Forskare
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RISE's accumulated knowledge in the field of cleaning and disinfection is evident from the services offered in the test and demo facility Cleaning Innovation.

The purpose of the testbed is to manage requirements for a small resource consumption in the form of water, chemicals, materials – while it is clean from microorganisms and dirt.

Read more about our services at:.

Eco-smart and effective cleaning and disinfection | RISE

ISO 17665 Validation of Sterilization Instructions | RISE

ISO 17664 Validating Instruction for Users for cleaning and disinfection | RISE

Division (OLD): Division Bioeconomy Division: Division Bioeconomy Infection control

Technical evaluation of air filters

Name of service (page headline, shown in promos – maximum of 70 characters incl. spaces): Testing of Air filters Lead (include SEO-words and the main benefits for your target groups. Stick to one paragraph, maximum 2-3 sentences):

RISE can offer technical evaluation of air filters. We mainly work with testing against the established standards such as ISO 16890 and EN 1822, but we also perform testing adapted to the customer’s requirements.

Purpose/Benefit:

RISE offers accredited tests of ventilation filters, which can be used to verify their products, used as a part of a product development process, or used as a basis for procurement.

Within the framework of P-labelling, we also offer long-term tests where the filters are evaluated with regards to filtration properties after being used in a real environment.

 

Method (what/which methods are used to perform the service):

Testing are conducted at RISE's laboratory in Borås within the testbed of Ventilation and Indoor environment. We have the possibility to evaluate ventilation filters according to the ISO 16890- and EN 779 standard. We also carry out long-term tests according to SP-Method 1937, which forms the basis for P-marking of ventilation filters. 

Delivery (what does the client get after performed service – e.g. a report, certificate etc.):

A technical report is provided and delivered for each testing. The preliminary results and data are presented based on the purpose of the testing. If the testing is a part of the P-marking, a certificate will be obtained with an approved implementation.

Delivery time:

According to tender

Area:
Construction
Energy
Preventive healthcare
Built environment
Contact person (Enter one name per field. Activated personal contact pages will appear automatically):
Tobias Eriksson, Ingenjör
Contact for air filter
Filterrig
Field measurements: No Price type: 1 Division: Do not use - Division Built Environment Preparation: No preparation required Link to order form: filter@ri.se Standards:

ISO16890

EN779

EN1822

SP-Metod 1937

ISO 29461-1

Certification and marking: Product certification Type of service:
Certification
Testing / Analysis / Evaluation
Instrument:
Barometers
Flow meters
Air flow / Gas flow
Humidity sensor
Particle counter
Thermometers
Pressure / Vacuum sensors
General area:
Gas flow
Humidity
Pressure and vacuum
Volume and flow
Order information: Contact us for more information by using filter@ri.se Divison (OLD): Do not use - Division Built Environment Delivery level: Accredited
tobias.eriksson@ri.se,filter@ri.se
/om-rise/verksamheten/uppdrag-styrning/policydokument/personuppgiftspolicy
Request for quote
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Construction Sekundär områdes navigation:
Metrology
Infection control
Tjänstetyp tagg: Provning

Biological Safety and Function

BioSafe
Biologic safety and function

We offer everything from biological analysis related to human health to providing solid advice regarding or taking responsibility for the biological evaluation of a product. We perform cell-and tissue-based, microbiological and animal based experiments, according to standards or customised, in order to evaluate function or safety of a product.

RISE has invested in a BD FACSLyric – a flow cytometer designed to enhance precision and quality in advanced cell analysis.The BD FACSLyric enables cost- and time-efficient analysis combined with precise isolation and characterization capabilities.

Laboratory testbeds (LT)
Västra Götaland Region

Benny Lyvén

Affärsutvecklare
+46 10 516 52 68 Read more about Benny
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Division: Division Bioeconomy

We use cell and tissue-based systems, microbiological systems and animal models, and perform the studies in well-equipped and quality-assured laboratories, e.g.: 

  • Cytotoxicity and skin irritation tests performed according to GLP 
  • Wound healing models in vitro and in vivo 
  • Cell adhesion and cellular uptake tests 
  • Gene expression studies 
  • Analysis of inflammatory markers 
  • Evaluation of biocompatibility according to ISO 10993 
  • Skin absorption tests 
  • Validation of in vitro test methods 
  • Infection control studies in vitro, ex vivo and in vivo 
  • Cancer inhibition screening assays in vitro 

We have good knowledge regarding regulatory requirements and are happy to give advice regarding the planning and scope of a biological evaluation, interpretation of results and advice for registration of products. 

Health and Life Sciences
Pharmaceuticals
Not applicable
2015

Address

Brinellgatan 4, Borås

Medtech Sekundär områdes navigation:
Metrology
Infection control

Legionella safe & energy efficient domestic hot water

Legionella safe domestic hot water
Shower

Energy optimization is central for sustainable development and domestic hot water temperature is important. A compromise between energy use and microbial safety is needed. In the project, the hypothesis that the limited water volume solution allows water temperature to be reduced without increasing the Legionella risk, was tested.

Project manager
Completed
Energy Infection control Chemical and biological analysis Resource-efficient cities Risk and safety Built environment Water
2016-2020
Division: Division Bioeconomy

Aim and goal

This project aimed at evaluating how a limited domestic hot water (DHW) volume at reduced temperature would affect the growth of Legionella and how such a system could be implemented in real buildings.

Challenge

One important aspect in sustainable building is to optimize energy consumption, with DHW temperature being one essential factor. The optimal DHW temperature is often a balance between energy demands and microbial safety, in particular the risk of Legionella spp. at temperatures below 50 °C. Methods to remove Legionella used today has been shown to last for a short time and give rise to e.g. problems with leakage due to damage on the DHW installations. There is therefore a need to investigate novel approaches to solve this problem.

Solution

In new building constructions and renewal projects it is important to design the DHW system correct to minimize energy consumption and lower the risk of Legionella. One such approach would be to use a small volume of DHW, e.g. 3 L, and to heat the water instantaneously when needed. This approach has been tested in Germany and Denmark, but further evaluations are needed under Swedish conditions. There is also a need to study the Legionella biofilm formation under controlled conditions in such a system to be able to assess the risks in a long-term perspective.

Effect

The investigated system could potentially provide a stronger Legionella protection, and simultaneously allow a reduction of the DHW temperature with substantial reduction in the energy consumption.

Charlotta Löfström

Senior Forskare
+46 10 516 67 30 Read more about Charlotta
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3. Good health and well-being
6. Clean water and sanitation
9. Industry, innovation and infrastructure
11. Sustainable cities and communities
19 partners representing technology suppliers, energy companies, consultants
Project end date: Water Sekundär områdes navigation:
Construction
Infection control

Visualization of cleaning effects in health care and food production

Analysis method to visualize cleanliness
Cleanliness

Reducing infections will give socioeconomic benefits. Cleaning is often done manually making it difficult to determine if it is enough. Standards to measure cleanliness is lacking. We develop an analytical method to provide a picture of the microbiological content on a surface after cleaning.

Project manager
Active
Infection control Chemical and biological analysis Food Preventive healthcare Service innovation
2018-2022
Division: Division Bioeconomy

Aim and goal

The project's goal is to develop a measurement method for studying dirt and microflora on surfaces to visualize the effects of cleaning methods and routines. The measurement method is intended to provide quick feedback to the user of the cleaning products and increase the motivation to clean efficiently. In addition, routines for the cleaning and effects of implementing some interventions are mapped into two case studies in hospitals and food production.

Challenge

There are major socio-economic benefits to reduce the spread of pathogenic viruses and microorganisms in homes, public environments, health care and food production. Here cleansing is crucial to prevent infection spread.

A large part of the cleaning is manual work, and it is often difficult for the person to decide whether the cleaning is enough. In addition, often there are no standards for measuring what is clean enough.

Solution

A good method for measuring the purity and presence of microorganisms, which provides quick feedback on the cleaning efficiency of the operator, would provide more efficient cleaning. In addition to this, the possibility of evaluating the types of microorganisms present on the surface and how they vary over time would be valuable to, for example, be able to see if a change in routines affects the levels and types of microorganisms., and thereby reduce infection spread.

In the project, flow cytometry (FC) is evaluated as a quick analysis method to get an overview of the composition and levels of microflora on surfaces. The method is used today for routine analysis of drinking water production and promising studies also show that the analysis can be automated, and the equipment miniaturized to be used directly by cleaning staff or operator.

Effect

Measuring cleaning efficiency faster and more efficiently, as well as an opportunity to evaluate the types of microorganisms present on surfaces in the patient room is an important part of patient safety work. In the food industry, this information allows for increased food safety and improved hygiene, resulting in less recalls and food waste.

Charlotta Löfström

Senior Forskare
+46 10 516 67 30 Read more about Charlotta
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3. Good health and well-being
9. Industry, innovation and infrastructure
11. Sustainable cities and communities
Project end date: Infection control Sekundär områdes navigation:
Metrology
Food
Service innovation

Eco-smart and effective cleaning and disinfection

Cleaning Innovation
Detergent

A test bed with a holistic approach to the efficiency aspects, as well as environmental aspects of cleaning and disinfection.

Laboratory testbeds (LT)
Not applicable

Lars Hamberg

Senior Forskare
+46 10 516 66 45 Read more about Lars
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Division: Division Bioeconomy

Cleaning Innovation is a test bed for the development of cleaning and disinfection. It provides independent evaluation of technologies, chemicals, materials, equipment and methods.

Among other things, the testbed consists of:

  • Pilot plants for closed and open cleaning/disinfection
  • Technical equipment for flexible pilot plant tests
  • Biofilm reactor
  • Methodology for identifying, tracking and managing biological and chemical dirt
  • Mobile and stationary cleaning facilities
  • Analytical equipment for the characterization of dirt and microbiological biofilm
  • Analytical equipment/methods for micro organisms
  • Methodology for mapping of cost (time, temp, etc.)
  • Graphics software (laser scanning, CAD layout)
  • Software for calculation/simulation of air currents, diffusion, cooling, heating
Energy and Clean Tech Health and Life Sciences Food and agriculture
Infection control Agriculture Climate neutral industry Chemical and biological analysis Life Science Food Medical devices Production and manufacturing Product safety
Not applicable
2016

Address

Frans Perssons väg 6, Gothenburg

Division (OLD): Division Bioeconomy Mer information:

Read more about our services:

Food Sekundär områdes navigation:
Production and manufacturing
Infection control

Materials for use in wet areas

Materials for use in wet areas
Testing of equipment for bathroom

The only facility in Sweden where research, testing, evaluation, damage investigations, calculations and certification are carried out in the field of materials for use in wet areas and water damage.

Isolated testbeds (IT)
Västra Götaland Region

Pontus Randén

Gruppchef
+46 73 020 85 20 Read more about Pontus
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Division: Division Materials and Industry

The test beds includes wet room and water damage area. A wide variety of things can be done, such as:

  • Testing according to many standardized methods, mainly according to ETAG 022 for pre-testing as the basis for certification
  • Special tests, for example: prefabricated bathroom modules, aids for disabled people, etc.
  • Damage investigations
  • Moisture calculations of different kinds of wet areas
  • Certification of wet room products and construction for use in wet areas (CE- and P-marking)
     

This unique environment makes it possible to investigate all possible scenarios in research and evaluation of construction for use in wet areas

Buildings and infrastructure
Construction
Not applicable
1990

Address

Brinellgatan 4, Borås

Construction Sekundär områdes navigation:
Metrology
Infection control
Materials and durability