County Down Businessmen Launch Rapid Covid Test Swab

NI Company Alpha PH launches first rapid swab test for Covid-19.

0
404

NI Company Alpha PH launches first rapid swab test for Covid-19.

  • 20,000 units ordered in three weeks –

Northern Ireland company Alpha PH has just launched the first rapid swab test for Covid-19 that gives test results within 15 minutes.

Alpha PH Director Kevin Sweeney from Castlewellan is set for a busy time ahead with his rapid testing Covid-19 kit.

The test has been brought to the NI market by three County Down businessmen who have developed a partnership with European bio-technology company, Alpha Pharma.

Accurate, fast and affordable, Alpha PH’s rapid swab test is conducted without the need for laboratory analysis; and in just over three weeks, the company has secured orders for 20,000 units from companies, sporting organisations and healthcare facilities across the UK and Ireland.

Alpha PH secured the UK and Ireland distribution rights from Alpha Pharma, and the NI company is now distributing two products, the VivaDiag SARS-CoV-2Ag rapid swab antigen test and the Iris VivaDiag COVID-19 IgM IgG rapid antibody test

Explaining how the distribution partnership developed, Alpha PH Director, Kevin Sweeney, who is from Castlewellan, and has 20 years’ working within healthcare and pharma, said: “As one of the leading bio-technology companies in the EU, Alpha Pharma is best known for its production and distribution of blood analysis systems, most commonly used in the detection and monitoring of diabetes. 

“Through a mutual connection, we heard about Alpha Pharma’s work back in April. Being based in Italy, the company had witnessed the devasting effects of coronavirus first-hand, and the business quickly pivoted its expertise, resources and technology to the trial and development of Covid-19 testing.”

After months of thorough research and trials, Alpha Pharma firstly launched its antibodies test in April, which has now been distributed to organisations, including hospitals and other health care facilities across the globe.

Kevin Sweeney added:  “Alpha Pharma’s first antibodies test is now widely used in medical settings and manufacturing in Italy and further afield, and we believe that these tests could really make a difference to public bodies and companies here in NI as we all try to navigate the future, ensuring safe workplaces and environments in the months ahead.”

The latest product to be introduced is its game-changing rapid swab test, and similar to the antibodies test, it also removes the need for costly laboratory analysis. 

Accuracy is paramount and the Alpha Pharma tests have been proven to deliver an 100% specificity for negative patients and sensitivity of up to 98% for positive patients.

Mr Sweeney said: “It has become clear that the widespread availability of accurate and appropriate diagnostic tests for Covid-19 is crucial to curtailing the spread of Covid-19 and living with this virus.

“These products can significantly help to prevent the spread of Covid-19 by diagnosing both symptomatic and asymptomatic people in a 15-minute frame.

“Working with Alpha Pharma, we have created a robust supply chain for the UK and Ireland with orders delivered within days. Customers have included sporting organisations, nursing home groups and food manufacturing businesses.”

“Testing is the way forward, and will enable our lives to move forward, whilst identifying and isolating those cases in our society to mitigate the spread of the virus”.

Recommended to be carried out by a healthcare professional, Alpha PH’s products are available now at :

www.alphatestkits.com

Featured products are the VivaDiag SARS-CoV-2Ag rapid test (swab test) for Covid-19, and the Iris VivaDiag Covid-19 IgM IgG rapid test (antibody test) which delivers a qualitative determination of lgM and lgG COVID-19 antibodies, indicating that a person has previously had the coronavirus.

Please visit:

 www.alphatestkits.com 

***

* Performance:  

–             Specificity 100% (for negative patients)

–             Specificity of up to 98% for positive patients, dependent on duration of infection 

–             Relative specificity: 100%

–             Relative sensitivity (4 to 10 days of lgG and lgM infection time): 81.25%

–             Relative sensitivity (11 to 24 days of lgG and lgM infection time): 97.1%

–             Accuracy (4 to 10 days of lgG and lgM infection time): 88.25%

–             Accuracy (11 to 24 days of lgG and lgM infection time): 98.3%             

ABOUT ALPHA PHARMA

ALPHA PHARMA is one of the leading bio-technology companies in the EU, best known for the production and distribution of blood analysis systems, most commonly used in the detection and monitoring of diabetes. 

Headquartered in Bitonto in the South West of Italy, Alpha Pharma develops leading predictive and precision medicine and technology. Products include the latest-generation, blood glucose meters and glycated haemoglobin and lipid profile analysers, which are distributed across the globe. Millions of people have benefited from Alpha Pharma’s diagnostic technology. 

In February, as Italy became the first European country to truly experience the devasting effects of the coronavirus, Alpha Pharma focused its expertise and resources, pivoting its technology to the development of Covid-19 testing.

Recommended for use by a healthcare professional, Alpha Pharma’s tests deliver accuracy, information and can significantly help to prevent the spread of covid-19 by diagnosing both symptomatic and asymptomatic people. 

CERTIFICATION

Alpha Pharma’s tests have been developed with safety and accuracy as paramount. Each test has undergone rigorous testing. The VivaDiag SARS-CoV-2Ag rapid test (antibodies test) and Iris VivaDiag COVID-19 IgM IgG rapid test (swab test) are manufactured in compliance with CE and WHO directives.

  •              Manufactured in compliance with CE directives
  •              Manufactured in compliance with WHO directives
  •             Registered with Italian Ministry of Health
  •              EUA (emergency use authorisation) granted by US Food & Drug Administration