The MHRA has renewed its commitment to the Early Access to Medicines Scheme (EAMS) which speeds up access to medicines for those with life-threatening or debilitating conditions gov.uk/government/cas… #ClinicalTrials

Validation of labeling systems and processes can be a minefield. Join the next @PRISYMID webinar on 24th May for advice and best practice. prisymid.com/webinars/true-… #MedicalDevices #ClinicalTrials #LabelingSolutions

Drug non-adherence can be costly and dangerous and these risks are amplified in a clinical trial. Clear and effective labeling can prove invaluable. medicalnewstoday.com/articles/takin… #ClinicalTrials

Interesting overview of the importance of infusion devices and how supply shortages have arisen during the pandemic med-technews.com/medtech-insigh…

Encouraging to see how decentralised trial models are being used in paediatrics to boost recruitment and retention through more patient-centric care and making greater use of technology clinicaltrialsarena.com/analysis/small… #ClinicalTrials

The pandemic has appeared to accelerate the adoption of decentralised #ClinicalTrials. An agile and flexible supply chain is essential to successful delivery. hitconsultant.net/2021/04/15/dec…

This is an interesting survey on the state of EU #MDR implementation and the challenges of compliance. medicalplasticsnews.com/news/one-year-… My colleague Richard Castle recently wrote a fantastic blog outlining five key recommendations for effective implementation. prisymid.com/blog/eu-mdr-ou…

Challenges in the supply chain and the resulting shortages mean that there is considerable interest in mixing and matching vaccines - offering a different vaccine as a second dose. Trial results are due in June 🤞 clinicaltrialsarena.com/analysis/covid…

A disruptive entrant to #pharma market built entirely on blockchain? It will be interesting to see how their decentralized model works in practice and their clinical trial technology. finance.yahoo.com/news/blockchai…

It is fantastic news that the EU portal and database for #ClinicalTrials is on track to go live next year, achieving one of the key deliverables of the 2014 Clinical Trial Regulation. europeanpharmaceuticalreview.com/news/151922/em… #ClinicalTrials

Diversity in clinical trials can be enhanced through patient-centric trials and greater trust in processes. Accessibility is another key issue and there are signs that decentralised trials could be part of the solution. appliedclinicaltrialsonline.com/view/steps-tow….

Great overview of the benefits of adopting additive manufacturing, including for the production of essential medical equipment and how this has been used to bridge supply issues during the pandemic. tctmagazine.com/blogs/guest-co… #MedicalDevices

Providing and maintaining product information online is just one of the key areas of compliance once EU MDR becomes fully applicable this month. This is a great whitepaper from @NetworkPartner5 exploring the role of eIFUs. networkpartners.com/resource/eifu-… #eIFU #IFU #MDR #MedicalDevices

Join my colleague Phil Dray and other industry experts as they share best practices of implementing a ‘validation ready’ cloud-based global labeling system in our webinar on 24th May. prisymid.com/webinars/true-…

Join my colleague Phil Dray and other industry experts as they share best practices of implementing a ‘validation ready’ cloud-based global labeling system in our webinar on 24th May. prisymid.com/webinars/true-…

There’s no denying it, product recalls are an expensive reality for many companies. However, some common labeling product recalls can be avoided. This free e-book discusses how you can strengthen your labeling infrastructure. prisymid.com/whitepaper/e-b…

We know that the pandemic has sped up the wider adoption of decentralized clinical trials so it was interesting to read a range of perspectives on which changes might become permanent #ClinicalTrials biopharma-reporter.com/Article/2021/0…

In case you missed it, the Medical Device Coordination Group recently updated its guidance on the practices European countries should follow until the Eudamed database goes live next year #MDR #MedicalDevices medtechdive.com/news/with-mdr-…

In Vietnam they are drafting new regulations for #MedicalDevices that will mean changes to #ClinicalTrials, manufacturing, marketing and advertising mondaq.com/life-sciences-…

The long-awaited EU #MDR comes into application today. If you're still working on ensuring your labeling function is compliant, please download our free practical checklist to assist your business operation. prisymid.com/infographic/eu…