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Covid-19

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Mondi safely packages QIAGEN’s SARS-CoV-2 test cartridge

08 Jul 2020
Yukta Arora
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QIAGEN is a leading global provider of molecular Sample to Insight solutions. The company recently launched a syndromic test cartridge kit for the QIAstat-Dx Analyser System that can identify the SARS-CoV-2 coronavirus within an hour. Designed for use in hospitals, clinics and laboratories, the company’s new QIAstat-Dx syndromic testing platform comes in the form of a compact, modular, table-top device into which multi-chamber cartridges containing test samples are inserted for analysis.

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International regulators provide guiding principles for COVID-19 clinical trials

03 Jul 2020
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EMA has endorsed a joint statement on prioritisation of COVID-19 clinical trials published by the International Coalition of Medicines Regulatory Authorities (ICMRA).
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Covid-19
effective and safe medicines

High demand for protective garments for the medical sector: Reifenhäuser converts another pilot line for production

02 Jul 2020
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The Covid-19 crisis puts global production capacity for hygiene products to a severe test. In March Reifenhäuser has temporarily produced metlblown to produce roughly one million face masks a day at its Technology Center. The company has now converted another pilot line for production. The first batch produces 110 metric tons of protective film for a global leading manufacturer for medical coveralls for use in hospitals. The increased demand is currently very high for coveralls worn to treat highly infectious coronavirus patients.
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Covid-19
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COVID-19 EMERGENCY

25 Jun 2020
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For this reason, it implemented all the indications provided for by the Shared Protocol on March 14, 2020 between the Government, Trade Unions and Trade Associations. In order to allow its employees and suppliers to access workplaces in compliance with the precautions that the current serious situation requires to adopt.

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Global regulators discuss data requirements for phase 3 trials of COVID-19 vaccines

25 Jun 2020
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Under the umbrella of the International Coalition of Medicines Regulatory Authorities (ICMRA), international regulators discussed COVID-19 vaccine development and the necessary evidence required for regulatory decision-making at the second regulatory workshop on COVID-19 vaccines.
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diverse populations
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Coronavirus: An update from the Meech team

23 Jun 2020
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The situation with the Coronavirus/COVID-19 is, as I’m sure you’re aware, constantly evolving. Our senior management team are meeting regularly to review the guidance we receive and the advice we give. We have also updated our procedures to ensure we are able to honour our commitments to our team and our customers. Our intention at this time is to maintain an uninterrupted supply chain, this will include functioning production, order processing and technical departments, along with a customer service support team.

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International regulators stress value of safe and effective vaccines

22 Jun 2020
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EMA has endorsed two statements about the importance, safety and effectiveness of vaccines published today by the International Coalition of Medicines Regulatory Authorities (ICMRA).
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confidence in vaccine safety and effectiveness.

Highlights of Management Board: June 2020 meeting

13 Jun 2020
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At its virtual meeting on 11 June, the Management Board was updated on how EMA is prioritising the response to the COVID-19 pandemic and what measures the Agency has put in place to tackle the crisis. The Agency and the European medicines regulatory network are currently operating under a network COVID-19 business continuity plan to ensure that core public and animal health regulatory activities, such as the authorisation, maintenance and supervision of medicines continue to be carried out during the pandemic and do not incur any possible delays.
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COVID-19: Information on the availability and protective measures at KURZ

11 Jun 2020
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Production is maintained in all of our 9 factories worldwide. In the KURZ plants and in our 25 sales branches all over the world, we can react quickly to regional fluctuations. The security and flexibility of raw material supply are also guaranteed thanks to our well-organized supplier network. We therefore currently see no restriction in our customers' delivery. At all of our locations, we have strengthened existing hygiene measures and regulations and made additional protective products such as disinfectants available. Our employees are instructed to comply with international standards.

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Latest data support continued use of ACE inhibitors and ARB medicines during COVID-19 pandemic

11 Jun 2020
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Recent observational studies of angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs, also called sartans) have not shown an effect of these medicines on the risk of becoming infected with severe acute respiratory syndrome coronavirus 2 (the virus causing COVID-19) and do not indicate a negative impact on the outcome for patients with COVID-19 disease. EMA therefore reiterates its previous advice that patients should continue to use ACE inhibitors or ARBs as advised by their doctors.
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