Sep 12, 2020

The rise of the COVID-19 test kit market

covid-19 testing kit
Global Market Insights
3 min
The rise of the COVID-19 test kit market
Research company Global Market Insights analyses the growing market for COVID-19 detection kits...

The ongoing COVID-19 pandemic has asserted a tremendous global impact in the past few months. One of the most crucial aspects to monitoring and controlling the spread of the virus is to conduct regular and thorough testing. As a result the COVID-19 detection kits market has gained immense attention as healthcare facilities and frontline workers look for robust testing solutions to detect the virus, with an expected growth rate of 17.3% by 2026. 

COVID-19 diagnostic testing is conducted under two approaches, including Real-Time Reverse Transcriptase PCR (RT-PCR), and Whole Genome Sequencing. While early days of the virus outbreak involved the sequencing approach for early documentation and as a tool for viral discovery, current coronavirus testing is largely conducted via the RT-PCR approach.

Many businesses across the globe have taken on the task of developing efficient coronavirus testing kits. For instance, Meridien Biosciences developed a “Master Mix”, which acts as a foundation for rapid COVID-19 testing. The test kit developed by the company works similarly to those for influenza detection. Once the “Master Mix” is shipped from Germany, the kits are assembled in China. These COVID-19 detection kits can yield results in around 45 to 60 minutes.

Prioritising those at high risk

Studies have revealed that elderly populations as well as those with existing comorbidities have a higher risk of mortality. In light of this, prioritizing testing for older populations is paramount. 

Health systems have been advised to provide COVID-19 diagnostic testing kits in settings other than the emergency department as much as possible. They have also been advised to use remote treatment options like telecare to carry out the screening process.

Since access to proper testing for high-risk populations is a significant challenge, many healthcare industry players are coming up with solutions to mitigate this problem. For instance,US-based TRHC (Tabula Rasa HealthCare) decided to provide its PACE (Programs of All-Inclusive Care for the Elderly) partners with COVID-19 detection kits through CareKinesis®, its national PACE pharmacy. 

This federal program, which is designed to offer comprehensive social and medical services to people aged 55 years and over, has expanded its remote care capabilities to administer these kits in people’s homes, minimising risk.

Addressing the need for effective testing

Prominent industry players have been working in collaboration with regulatory authorities, implementing strategies to quickly address the demand for effective testing solutions. Mylab Discovery was the first company in India to earn approval for its COVID-19 diagnostic kits. The kits have received CDSCO (Central Drugs Standard Control Organisation), India’s equivalent to the USA’s FDA approval. 

PepsiCo India has also been distributing testing kits to sites across the nation. The kits are being purchased and distributed by FIND (Foundation for Innovative New Diagnostics), supported by PepsiCo’s funding and ICMR (Indian Council of Medical Research) approval.

Meanwhile, organisations around the world continue working towards finding accurate, fast testing solutions. One of the latest developments is a 20-second saliva test that has just had its first round of field testing among employees of the UK’s Heathrow airport. It uses a digital microscope and AI software to search a mouth swab sample for signs of the virus. 

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Jun 19, 2021

Driving sustainability in medical device production

George I’ons
5 min
George I’ons, Head of Product Strategy and Insights at Owen Mumford Pharmaceutical Services on how technology is driving sustainability 

Environmental protection and stewardship are rapidly rising to the top of the corporate agenda and medical device businesses are no exception. The healthcare sectors of the United States, Australia, Canada, and England combined emit an estimated 748 million metric tons of greenhouse gases each year, an output greater than the carbon emissions of all but six nations worldwide. In order to curb this situation various European standards have been introduced. 

The Waste Electrical and Electronic Equipment (WEEE); Restriction on Hazardous Substances (RoHS); Registration, Evaluation, and Authorisation of Chemicals (REACH) and the Energy Using Products (EuP) regulations have all significantly altered manufacturing processes, specific labelling, compliance with disposal restrictions, and creation of instructions for end-of-life management and recycling.

At the moment many medical devices are currently exempt from these regulations but several directives, including RoHS and WEEE, are in the process of being reviewed and could be applicable in future. This is especially relevant for devices that are ‘connected’ and have a digital monitoring component which then brings them under the regulatory purview of authorities that govern devices with electronic components.

Safety, Usability and Sustainability

While medical device manufacturers have been working to respond to increasing demand for environmental sustainability from the market, they also have to contend with a key element of their mission: to ensure safety and usability to healthcare workers and patients. Parenteral and other invasive devices are strictly regulated to help reduce the risk of Healthcare Acquired Infection which typically runs as high as 5% and 8% in most developed countries, according to the European Centre for Disease Prevention and Control. As a result, they typically contain disposable single-use plastic elements.

At the same time, many hospitals and purchasing organisations have started to recognise that sustainable purchasing practices play a pivotal role in reducing costs over time. Many GPOs have appointed and empowered Senior Directors of Environmentally Preferred Sourcing who are successfully implementing the sustainable purchasing business case. In addition global pharmaceutical companies are increasingly creating senior positions with sustainability objectives as key to the role.

Medical device disposal is a particularly burning issue; generally carried out through incineration in the EU, it typically releases nitrous oxide, as well as known carcinogens including polychlorinated biphenyls, furans and dioxins. Some of the strategies trialled by manufacturers to reduce waste matter destined to incineration include sterilisation and reprocessing.

Sterilisation, however, falls short on the environmental front, and may consume more energy and produce more emissions than incineration itself. In the United States for example, 50% of all sterile medical devices are sterilised with ethylene oxide but since this method releases harmful emissions, the US Food and Drug Administration is now encouraging the development of new methods or technologies. Many other established sterilisation methods use glutaraldehyde that is not only harmful to the environment but also tends to be regulated by strict usage and disposal rules such as COSSH guidelines.

Focus on Recycling

The outlook on recycling is changing significantly thanks to new research and technologies enabling, for example, monomer extraction. Recycled polymers can be broken down to their constituent monomers promoting an almost limitless recyclability of some polymers. In addition to this, Polyvinyl chloride (PVC), renewable polyethylene and polyethylene terephthalate (PET) can be recycled several times without losing critical properties.

Reducing the impact of packaging can also significantly reduce the materials that need to be dealt with through either waste or recycling. Packaging manufacturers are decreasing packaging volume by favouring sealed trays instead of pouches, laser-etching instructions directly on to the tray where regulation permits it, or reducing the number of components required overall. In addition to this, for recycling plans to be successful it important to have a full understanding of the practices surrounding device use and to establish, where possible,  closed loop recycling systems that recover the waste materials from hospitals or patients and bring them back into the recycling process.

Sustainable Manufacturing: Technology and Research

Greater employment of fast degrading plastics or material from other sources is a key strategy to reduce harmful pollutants both at production and disposal stage. Bio-based materials can in fact offset the carbon emitted during processing as the monomer source grows, and a growing range of sources for bio based monomers -such as wood pulp or sugar cane- is available. However, when assessing the most suitable material for a part, the entire lifecycle of the product needs to be considered. For example: bio-degradable polymers can contaminate a recycling stream and emit methane when incinerated.

The use of environmentally friendly materials should also be supported by an increase in clean renewable energy sources. Lower energy consumption means fewer carbon emissions but also financial savings, making this an appealing measure for manufacturers. New technologies are proving a major gamechanger on this front, helping manufacturers marry their environmental stewardship with cost savings and efficiency.  3D printing, for example, can help develop optimum product moulds more quickly, refining production parameters to minimise raw materials volumes and maximising output productivity.

Similarly, ‘digital twin’ production software uses inline sensors to create a virtual, real-time mirror of the production environment to enable inline refinements. The objective is to achieve “zero defect”, waste-free manufacturing. In addition to this, LEAN manufacturing methodologies are already helping to optimise inventory management and reduce overproduction. 

Sustainability by Design

It is increasingly clear that effective environmental sustainability in the medical device sector cannot exist without a full view of the product life cycle from concept development, material selection, design and engineering to manufacturing, packaging, transportation, sales, use, and end-of-life disposal. These evaluations are typically made for factors such as manufacturing efficiency, time to market, or safety and regulatory compliance, packaging and transportation costs, but should be extended to energy efficiency and environmental impact by means such as life cycle analysis.  

In addition to this, with devices rapidly becoming more digitally connected, developers need to be aware that the costs of disposable electronics would simply not be viable, or indeed acceptable in the light of electronics disposal regulations. Design therefore should focus on creating a simple, repeatable interface between the two component sections so as not to impair the functionality or efficacy. As reducing waste and harmful emissions continues to exert businesses and governments globally, the medical devices industry cannot stand by. The environmental but also commercial implications of inaction are too serious and the array of solutions now available is exciting and diverse.

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