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med
duoTM

A platform for advanced multi-target testing with independent antigen and antibody detection enabling interference-free results.

One Platform. Any Combination.

The MEDDUO™ platform is designed to generate multiple results within the same device. It supports defined combinations of antibody and antigen targets as well as multiplex detection of up to eight (8) antibody or antigen analytes within one assay. The platform incorporates a dual-window read-out design that physically separates antigen and antibody detection pathways. This separation enables independent assay workflows, supports clear result interpretation, and prevents cross-interference between antigen- and antibody-based assays.

  • Immediate results

    No waiting time, results do not vanish.

  • Reliable accuracy

    Achieves high TP testing performance across multiple specimen matrices.

  • Antigen and antibody detection

    Dual-chamber design enables interference-free antigen and antibody results.

  • No equipment or refrigeration required

    Stores at room temperature (2–30 °C / 35–86 °F) with a 12-month shelf life.

  • Easy to use and interpret

    Simple procedure with instant, easy-to-read results, no special training required.

  • Ideal for any setting

    Works with serum, plasma, and whole blood (venipuncture or fingerstick)

medduo side

Dual-Window Formats

In contrast to conventional single-window RVF cartridges, the MEDDUO™ platform utilizes differentiated buffer volumes, multiple reagent vials, and two independent read-out windows. This architecture enables flexible assay configuration while maintaining separation of detection chemistries. The two read-out windows can be configured in different modes:

t1 t8 ab
Dual Antibody Testing

both windows configured for antibody detection

t1 t8 ag
Dual Antigen Testing

both windows configured for antigen detection

t1 t4 ab t5 t8 ag
t1 t8 ag
Dual Antigen Testing

both windows configured for antigen detection

From sample to results

in three simple Steps

Testing doesn’t have to be complicated. Our intuitive three-step process ensures instant, consistent results with minimal effort. 
In this example, the right read-out window is configured for antigen detection and the left read-out window for antibody detection.

blood
Pour specimen

Add whole blood specimen to buffer in vial 1. 
Perform this step once only.

Antigen Antibody
medduo a gen1
Add sample to lyophilized vial

Using the supplied disposable pipette, add 10 drops from Step 1 to the lyophilize vial, mix to dissolve.

medduo a gen step2
Pour lyophilized content

Pour the contents of the lyophilized vial onto the right reaction window.

medduo blood
Pour specimen

Add whole blood specimen to buffer in vial 1. 
Perform this step once only.

medduo step3
Cap and Pour buffer

Place the InstantGold™ cap on the left reaction window and pour buffer onto it.

For a similar procedure, watch the Miriad® multiLinx™ HIV/HCV/TP Antibody & HBsAg/HBeAg Antigen video (Youtube, 5:05 min).

medduo2
Pour specimen

Add serum, plasma specimen to buffer in vial 1. Perform this step once only.

Antigen Antibody
ps2
Add specimen

Add specimen and mix to reconstitute the lyophilized material until fully dissolved.

medduo serum
Pour contents

Pour the contents of the lyophilized vial onto the right reaction window.

ps
Add sample

Pour the remaining specimen from vial 1 onto the left reaction window.

medduo step3
Cap and Pour buffer

Place the InstantGold™ cap on the left reaction window and pour buffer onto it.

For a similar procedure, watch the Miriad® multiLinx™ HIV/HCV/TP Antibody & HBsAg/HBeAg Antigen video (Youtube, 5:05 min).

Explore your options with us

Interested in learning more about the MEDDUO™ platform, developing a custom assay, or exploring new testing concepts? We welcome your inquiry. Please contact us for further information.

Contact us

Frequently Asked Questions

How does the dual-chamber technology improve result clarity?

Dual-chamber technology separates antigen and antibody reactions into two independent test areas, preventing them from affecting each other. In some single-chamber assays that use biotin-streptavidin binding chemistry, elevated biotin (vitamin B7) levels in patient samples can disrupt assay performance and lead to unclear or inaccurate results. By physically separating antigen and antibody detection into independent chambers, MEDDUO™ reduces the risk of such interference and helps ensure clear, reliable, and interpretable results for combination antigen/antibody testing.

How does MEDDUO™ differ from Multiplo®?

Multiplo® provides a single integrated readout for multi-parameter infection screening, ideal for broad public health testing. MEDDUO™, by contrast, uses a dual-window system that separates antigen and antibody detection, providing clear results without cross-interference and making it the preferred platform for next-generation antigen/antibody combination assays.

What tests are currently available on the MEDDUO™ platform?

The MEDDUO™ platform is MedMira’s dual-window RVF cartridge architecture. MultiLinx™ assays represent multiplex test configurations that may be implemented on MEDDUO™ or standard RVF cartridges. Certain RUO assays such as HIV-HCV-TP-HBsAg-HBeAg distributed through partners are based on licensed MedMira technology and represent earlier-generation implementations.

Is the MEDDUO™ platform limited to specific analyte combinations?

No. The MEDDUO™ platform is designed as a configurable system that supports a wide range of antibody and antigen combinations. Assay configurations can be adapted based on target selection and application requirements. For further information or specific assay inquiries, please contact us.
Contact us

What is RVF technology™?

RVF (Rapid Vertical Flow) is a flow-through technology that captures specific biomarkers from blood, serum, or plasma samples on a specialized membrane, delivering instant visual results.
Learn more

Privacy Policy

Last updated: April 20, 2026

MedMira Inc. (“MedMira”, “we”, “us”, or “our”) is committed to protecting personal information in accordance with applicable privacy laws, including the Personal Information Protection and Electronic Documents Act (PIPEDA) in Canada, as well as applicable United States and international privacy requirements.

This Privacy Policy describes how we collect, use, disclose, and safeguard personal information through our website. Our website is primarily informational in nature and does not provide user accounts, applications, or diagnostic services.

1. Personal Information We Collect

We collect personal information only where it is voluntarily provided by you. “Personal information” means information about an identifiable individual. The types of personal information we may collect include:

a) Contact Forms
When you submit an inquiry, we may collect your first and last name, email address, phone number (optional), organization (optional), inquiry details, selected topic, and message, as well as your self-identified category (e.g., partner, healthcare provider, researcher, investor, media, or other).

b) Newsletter Subscription
If you subscribe to receive updates, we may collect your email address and, where provided, your category or area of interest.

c) Communications
We may retain records of communications you send to us, including emails and inquiries, in order to respond to you and maintain appropriate business records.

We collect personal information directly from you and do not knowingly obtain personal information from data brokers or unrelated third-party sources.

If you provide personal information relating to another individual, you represent that you have the authority to do so and that such information may be used in accordance with this Privacy Policy.

We do not intentionally collect sensitive personal information or collect more information than necessary for the purposes described herein.

2. Purposes of Collection and Use

MedMira collects and uses personal information for limited and legitimate business purposes, including responding to inquiries, communicating with you, providing information about our company and activities, delivering newsletters or updates where you have opted in, maintaining internal records, and complying with applicable legal and regulatory obligations.

We do not use personal information for profiling, automated decision-making, or targeted advertising.

3. Consent

By submitting personal information to MedMira, you consent to its collection, use, and disclosure as described in this Privacy Policy.

Where required by applicable law, you may withdraw your consent at any time, subject to legal or contractual restrictions and reasonable notice. Withdrawal of consent may limit our ability to respond to your inquiry or provide requested information.

4. Cookies and Similar Technologies

MedMira’s website does not use cookies, analytics tools, or tracking technologies for advertising or behavioral tracking purposes.

However, our website may include content or links to third-party platforms, such as LinkedIn, X (formerly Twitter), or YouTube. Interaction with such content (including embedded media or external links) may result in those third parties placing cookies or using similar technologies on your device.

MedMira does not control and has no access to data collected through such third-party technologies.

5. Disclosure of Personal Information

MedMira does not sell, rent, or trade personal information.

We may disclose personal information to third parties only in limited circumstances, including to service providers acting on our behalf (such as email distribution providers), who are contractually required to protect the information and use it only for the intended purposes.

We may also disclose personal information where required by law, regulation, legal process, or to protect the rights, property, or safety of MedMira or others, or in connection with a corporate transaction where permitted by law.

6. Third-Party Websites and External Services

Our website may contain links to or integrations with third-party services, including but not limited to Google Maps, SEDAR (System for Electronic Document Analysis and Retrieval), PubMed, LinkedIn, X (formerly Twitter), and YouTube.

These services are operated by independent third parties. When you access or interact with such services, your personal information may be collected and processed directly by those third parties in accordance with their own privacy policies.

MedMira does not control and assumes no responsibility or liability for the privacy practices, content, or data handling activities of third-party services. Accessing such services is at your own risk.

7. Data Retention

We retain personal information only for as long as necessary to fulfill the purposes for which it was collected, including responding to inquiries, maintaining communication records, and providing newsletters.

Personal information associated with newsletter subscriptions is retained until you unsubscribe. We may retain information for longer periods where required to comply with legal obligations or to establish, exercise, or defend legal claims.

8. Safeguards and Security

MedMira implements reasonable administrative, technical, and organizational safeguards appropriate to the sensitivity of the information to protect personal data against loss, theft, unauthorized access, disclosure, copying, use, or modification.

However, no method of transmission over the Internet or electronic storage is completely secure. While we take appropriate steps to protect personal information, we cannot guarantee absolute security, and any transmission of information is at your own risk.

9. Cross-Border Transfers

MedMira is headquartered in Canada but may engage service providers located in other jurisdictions, including the United States. As a result, personal information may be transferred to and processed in jurisdictions outside your country of residence.

Such jurisdictions may have different data protection laws and may permit access by governmental authorities under applicable laws. By providing your personal information, you consent to such transfers where permitted by law.

10. Your Rights and Choices

Subject to applicable law, you may have the right to access, correct, or request deletion of your personal information, withdraw your consent to processing, or opt out of receiving communications.

To exercise your rights, please contact us using the contact details below. We will respond to requests in accordance with applicable legal requirements.

11. Children’s Privacy

Our website is accessible to individuals of all ages but is not specifically directed at children. We do not knowingly collect personal information from children without appropriate consent.

If you believe that a child has provided personal information to us, please contact us so that we can take appropriate steps to remove such information where required.

12. Limitation of Liability

To the fullest extent permitted by applicable law, MedMira disclaims liability for the privacy practices, actions, or omissions of third parties, including external websites and service providers not under our direct control.

13. Changes to This Privacy Policy

MedMira reserves the right to update or modify this Privacy Policy at any time. Any changes will be posted on this page with a revised “Last updated” date. Continued use of the website following such changes constitutes acceptance of the updated Privacy Policy.

14. Contact Information

For questions, requests, or concerns regarding this Privacy Policy or our data practices, please contact:

MedMira Inc.
155 Chain Lake Drive, Suite 1
Halifax, Nova Scotia B3S 1B3
Canada

Email: info@medmira.com
Phone: +1 (902) 450 1588
Toll Free: +1 (877) 633 6372

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Third Party Sites

As a convenience to you, MedMira may provide, on this Site, links to websites operated by other entities. If you use these sites, you will leave this Site. If you decide to visit any linked site, you do so at your own risk and it is your responsibility to take all protective measures to guard against viruses or other destructive elements. MedMira makes no warranty or representation regarding, and does not endorse, any linked Web sites or the information appearing thereon or any of the products or services described thereon. Links do not imply that MedMira or this Site sponsors, endorses, is affiliated or associated with, or is legally authorized to use any trademark, trade name, logo or copyright symbol displayed in or accessible through the links, or that any linked site is authorized to use any trademark, trade name, logo or copyright symbol of MedMira or any of its affiliates or subsidiaries.

External Links to the Site

All links to the Site must be approved in writing by MedMira, except that MedMira consents to links in which: (i) the link is a text-only link containing only the name “MedMira“; (ii) the link “points” only to www.medmira.com and not to deeper pages;(iii) the link, when activated by a user, displays that page full-screen in a fully operable and navigable browser window and not within a “frame” on the linked website; and (iv) the appearance, position and other aspects of the link may neither create the false appearance that an entity or its activities or products are associated with or sponsored by MedMira nor be such as to damage or dilute the goodwill associated with the name and trademarks of MedMira or its Affiliates. MedMira reserves the right to revoke this consent to link at any time in its sole discretion.

Limitations of Damages

YOU EXPRESSLY AGREE THAT USE OF THE SITE IS AT YOUR SOLE RISK. NONE OF MEDMIRA NOR ANY OF ITS RESPECTIVE DIRECTORS, EMPLOYEES, AGENTS OR OTHER REPRESENTATIVES WILL BE LIABLE FOR DAMAGES, CLAIMS, EXPENSES OR OTHER COSTS (INCLUDING WITHOUT LIMITATION LEGAL FEES) ARISING OUT OF OR IN CONNECTION WITH THE USE OF, OR INABILITY TO USE, THE SITE OR ANY INFORMATION CONTAINED ON IT, OR ANY HYPERLINKED WEBSITE, WHETHER CLAIMED IN CONTRACT, NEGLIGENCE OR ANY OTHER CAUSE OF ACTION. THIS IS A COMPREHENSIVE LIMITATION OF LIABILITY THAT APPLIES TO ALL DAMAGES OF ANY KIND, INCLUDING (WITHOUT LIMITATION) COMPENSATORY, DIRECT, INDIRECT, EXEMPLARY, PUNITIVE AND CONSEQUENTIAL DAMAGES, PERSONAL INJURY, LOSS OF PROGRAMS OR DATA, INCOME OR PROFIT, LOSS OR DAMAGE TO PROPERTY AND CLAIMS OF THIRD PARTIES.

Changes

MedMira reserves the right, at its sole discretion, to change, modify, add or remove any portion of this Agreement in whole or in part, at any time. Changes in this Agreement will be effective when notice of such change is posted. Your continued use of the Site after any changes to this Agreement are posted will be considered acceptance of those changes. MedMira may terminate, change, suspend or discontinue any aspect of the MedMira Site, including the availability of any features of the Site, at any time. MedMira may also impose limits on certain features and services or restrict your access to parts or all of the Site without notice or liability. MedMira may terminate the authorization, rights and license given above and, upon such termination, you shall immediately destroy all Materials.

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Committed to quality
Certified & Proven Quality

Our quality management system is ISO 13485:2016 certified, compliant with the United States Food and Drug Administration’s current Good Manufacturing Practices (cGMP: Quality System Regulation Part 820 of CFR Title 21, Volume 8), European Union’s Directive 98/79/EC on in vitro diagnostic medical devices, and Health Canada Medical Device Regulations (SOR/98-282).

Additionally, we adhere to ISO 14971 (Application of Risk Management to Medical Devices) and ISO 2859 (Sampling Procedures for Inspection by Attributes). Certification and compliance to these requirements attests to our ability to maintain the highest standard of quality in medical device manufacturing, product development and corporate conduct.

Our products have been approved by regulators and UN agencies worldwide.

FDA

Health Canada

International Trade Centre (ITC)

Pan American Healtch Organization (PAHO)

UN Development Programme (UNDP)

UN Office for Project Services (UNOPS)

UN Office at Vienna (UNOV)

UN Population Fund (UNFPA)

United States Agency for International Development (USAID)

CFO & Head of Commercialization

Markus Meile

Markus joined MedMira in 2010, and moved into the role of Chief Financial Officer in 2014.

He previously served on the Company’s Board of Directors, as a member of the Audit Committee, and as the Senior Director of International Markets.

Prior to joining MedMira, Markus worked with a number of financial institutions in Switzerland, England, and Hong Kong. He holds a BSc from Royal Holloway University of London and has studied business management, strategic planning, investment and accounting at business school in Zurich. Previously, Markus worked in the medical device industry in Africa, Asia Pacific, and Europe.

He will combine his financial expertise with his broad range of international business knowledge to build financial and corporate strategies supporting MedMira’s continuing growth and increasing shareholder value.

Director of the Audit Committee, Nomination and Compensation Committee

Jianhe Mao

Jianhe Mao is the owner of Unipec, a consulting firm based in St. Gallen, Switzerland. Unipec focuses on helping European companies enter the Chinese market, through operational restructuring and ownership and management optimization.

In addition to leading Unipec, Mr. Mao is involved in several industrial projects and start-up ventures including Monsatec AG, a new company bridging the gap between laboratories and clinics with a cold plasma medical device. He serves on the boards of several European companies and is regarded as a trusted expert in legal cases, corporate corruption, operational turnarounds, and mergers and acquisitions.

Mr. Mao began his career as a project engineer and has gained experience in business development and real estate investment. He holds M.E. from Ruhr University Bochum.

CEO, Co-Founder & Co-Inventor

Hermes Chan, D.Sc. (h.c.)

Hermes Chan, our Chief Executive Officer and Co-Founder, leads our passionate and committed team in driving the strategic direction and growth of MedMira.

Hermes, who was named BioScience Innovator of the Year by The Economist in 2007, is the inventor of our patented rapid flow-through diagnostic technology platform.

Since the company’s inception in 1994 Hermes has held progressively senior management roles including Research Scientist, General Manager, Senior Vice President, and Chief Operating Officer.

Prior to creating MedMira, Hermes worked with another Canadian biotechnology company in the diagnostics research sector.

Chair member of the Audit Committee, Nomination and Compensation Committee

Steven Cummings

Mr. Steven Cummings is the Founder & President of Cambridge Financial Services, one of the leading full service accounting, tax, and business advisory firms in Nova Scotia.

Under Mr. Cummings leadership, Cambridge Financial has earned an enviable reputation among businesses and industry for a commitment to high standards. Along with his leadership responsibilities at Cambridge Financial Services, Mr. Cummings was engaged as MedMira’s interim Chief Financial Officer in 2007.

With more than 30 years of financial and entrepreneurial experience, Mr. Cummings is a frequent guest speaker on issues surrounding provincial taxation, taxation of seniors, and business ownership

Intellectual property

China

ZL02819646.5

Rapid Diagnostic Device and Assay

Intellectual property

European union

EP1417489

Rapid Diagnostic Device and Assay

EP1328811

HCV Mosaic Antigen Composition (2021)

Intellectual property

USA

9,164,087

Rapid Diagnostic Device, assay and multifunctional Buffer

9,086,410

Downward or vertical flow diagnostic device and assay

8,025,850

Rapid Diagnostic Device, Assay and Multifunctional Buffer

8,287,817

Rapid Diagnostic Device, Assay and Multifunctional Buffer

8,586,375

Rapid Diagnostic Device, Assay and Multifunctional Buffer

7,531,362

Rapid Diagnostic Device, Assay and Multifunctional Buffer

D706945

Diagnostic Device

D706466

Diagnostic Device

11,353,450

Analyte Detection Using Raman Spectroscopy

Intellectual property

Canada

CA2,493,616

Rapid Diagnostic Device, Assay and Multifunctional Buffer

CA2,740,902

Downward or Vertical Flow Diagnostic Device and Assay

CA2,949,634

Analyte Detection Using Raman Spectroscopy

MiROQ Vision

Handheld Device

A future concept built on the same MIROQ technology, designed to deliver lab-grade precision in the palm of your hand.

We envision a future where testing can happen anywhere, anytime – from hospitals and clinics to remote regions or even at home – enabling early disease detection and turning knowledge into real impact. No large equipment or complex infrastructure required.

For: Doctor’s offices, small and mobile clinics

Future application: Home use

Connectivity: Bluetooth, Wifi and USB