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BioAge Labs said the potential safety problem was observed in some who received experimental drug azelaprag, which is being tested as a monotherapy and in combination with Eli Lilly obesity medication Zepbound. No safety signals were observed in those who received Zepbound alone.
The self-medicating plant movement sits at the intersection of empowerment and misinformation. On the other, it raises alarms about safety, oversight, and the risk of delayed care. The post The Rise of Plant-Based Self-Medication and What Healthcare Must Do Next appeared first on MedCity News.
In the same way that airbags were a natural evolution of vehicle safety technology, seamless, RFID-based systems are the next evolution of medication management technology.
The Clarifying Remanufacturing to Protect Patient Safety Act was introduced by Reps. Scott Peters (D-CA), Kim Schrier (D-WA), and John Joyce (R- PA) to clarify the meaning of medical device remanufacturing and empower the FDA to educate company technicians so they know if they’ve crossed the line into a regulated activity. .
The sourcing of commercial drugs for use in clinical trials either as a comparator, rescue or co-medication can be a complex process. Choosing the right partner with global sourcing, regulatory, quality and clinical packaging expertise can provide the necessary guidance to help sponsors successfully navigate these challenges.
Medical device companies that leverage today’s technology to better share and track product and safety information will outpace rivals and gain a competitive edge. The post Medical Device Innovation: Transforming The Workplace appeared first on MedCity News.
In todays rapidly advancing healthcare landscape, the demands placed on medical professionals are greater than ever. With new medical devices, surgical techniques, and treatment protocols emerging constantly, the need for effective, efficient, and scalable training methods has become paramount. billion by 2025.
The post From Recalls to Reliability: Tools to Ensure Software Safety in MedTech appeared first on MedCity News. Cutting-edge technology empowers developers to proactively detect and mitigate issues before they cause problems, reducing recalls and fostering trust in the industry.
While the approach to patient and treatment safety is crucial, there is a notable shift towards processes centered around patients and healthcare professionals. The post Beyond Engineering: Integrating UX for Safer and More Efficient Medical Products appeared first on MedCity News.
Human tissues, coupled with AI that can deal with terabytes of data will blow mice models out of the water. With animal testing requirements finally removed, the pharma industry and its constituents can hope for faster innovation.
Greater collaboration among healthcare providers, medical device manufacturers, and lawmakers and regulators will lead to predictability and consistency in cybersecurity management. Together, we can make even greater strides toward patient safety and a more secure and sustainable healthcare system.
While there are many consumer technology and electronic products for which the right to repair ideology may not have much of a safety risk, or perhaps even be beneficial, life-saving medical devices should not be among them.
From Ted Talks to the medical sales podcast! In this episode, he discusses the essential sales skills required for success as a medical sales representative. Tune in now and unlock the sales skills that will propel your career in medical sales. Welcome to the Medical Sales Podcast. Welcome to the Medical Sales Podcast.
There is growing and coordinated momentum behind the goal of ensuring connected medical devices improve people’s lives without introducing them to cybersecurity threats and associated safety risks. There also is a proven playbook for implementing the type of multi-layered, security-by-design strategies these initiatives advocate.
Patient safety and lack of autonomy are two of the biggest factors driving so many clinicians away from the medical field, according to a new EY report.
American Medical Association President Dr. Jesse Ehrenfeld said this is a “terrible idea.” He argued that throwing other professionals into physicians’ roles will have poor ramifications of patient safety. In his view, the industry should focus on uplifting strong interprofessional care teams.
Are you considering importing medical device? Or else looking to manufacture medical equipment in the United States? It regulates all medical devices in the United States. It is essential to understand the FDA’s definition of a medical device. You need to know how the agency classifies medical devices.
Critical applications, medical devices, protected health information (PHI), patient safety, and lives are all at risk when extended downtime occurs. The question is, are you and your team prepared?
But its influence on healthcare is especially significant; it is transforming the design and prototyping process of medical equipment. The immersive features of VR medical device development provide efficiency, safety and creativity.
VR training enables medical device maintenance personnel to practice and refine their skills without the risks associated with live equipment. As technology advances, VR training is becoming increasingly relevant, ensuring that maintenance teams are well-prepared to tackle the complexities of modern medical devices.
One of the major lessons learned during the pandemic is that hospitals and medical facilities are not always the safest places to recover, especially for seniors and those living with chronic conditions. Compounding this issue is that 85% of seniors in the U.S. live with one or more chronic conditions. With the United States being home to 55.8
The guidelines address the safety, effectiveness or quality of these medicines. With the appropriate safeguards in place, artificial intelligence has transformative potential to advance clinical research and accelerate medical product development to improve patient care.
Radio frequency identification (RFID) not only helps hospitals boost their medicationsafety standards, as it also allows clinicians to continue to provide quality patient care.
Medical reps in Malaysia don’t just sell products – they educate. From explaining how a medication works to addressing patient concerns, reps play a vital role in bridging the gap between healthcare providers and patients. The Role of Medical Reps in Patient Education Patient education isn’t just about handing out brochures.
VR environments can vary widely, ranging from realistic simulations of real-world settings, such as a medical operating room or a laboratory, to fantastical or imaginary worlds limited only by the imagination of the creators. Trends indicate a shift towards personalized and interactive experiences.
For life sciences organisations, particularly those with AI in medical devices, diagnostics and drug discovery, concerns have been raised as to whether the complexity and uncertainty of the regulatory landscape could hinder innovation in Europe.
But, the fact is the medical industry is growing at a faster pace with AI and VR technologies. Implementing emerging technologies for the future of medical training is most welcome. Medical training will be implemented via VR and emerging technologies. Importance: VR is already creating a milestone in the medical industry.
3D medical animation has become a revolutionary tool in today’s fast-paced healthcare environment, where clarity and accuracy rule. 3D medical animation remarkably precisely closes the communication gap between explaining how a new medical gadget works or simplifying the chemical mechanism of action for a medication.
Before starting her own business, Rebecca Kinney had 15 years of experience, seven of which were spent in the field of sterile processing and the other eight in medical sales. To Rebecca, starting her own medical branding business was a culmination of her medical sales skills. — Watch the episode here.
The first good manufacturing practice (GMP) registration of a UK pharmaceutical facility for high Δ9-tetrahydrocannabinol (THC) cannabis active pharmaceutical ingredient (API) has been granted since the legalisation of medical cannabis in 2018. Authorising medical cannabis in the UK.
Award-winning health and wellness advertising agency AbelsonTaylor Group received the inaugural ACE Aspire Award for its employee Psychological Safety Initiative from the Healthcare Businesswomen’s Association (HBA). In 2022, AbelsonTaylor developed and implemented a large-scale, ongoing Psychological Safety initiative for its 300 employees.
The medical device sales field in Malaysia is one of the most dynamic and rewarding sectors within healthcare. Here are 10 little-known facts about medical device sales jobs in Malaysia to help you navigate and succeed in this exciting field. The Sales Cycle Can Be Longer Than Expected Selling medical devices is often a long-term game.
Three key medicine regulatory bodies from the UK, US and Canada have collaborated to publish five guiding principles for machine learning-enabled medical devices MLMDs. The aim is to remove the regulatory burden of reassessment following certain changes and updates to a medical device by a manufacturer.
A paper published in the Journal of Pharmaceutical Research International has reviewed microbiological testing for medical devices and described their applications and challenges. Medical devices are essential tools for diagnosing, monitoring and treating a variety of conditions. Sharma et al.
9ine: Searches for specific medical terms have increased, indicating that people don’t necessarily understand common medical terms. 10en : The most consumed pages on most pharma websites is safety information and pages that offer co-pay cards as people try to save money on Rx’s. 2020 trend concept.
The US Food and Drug Administration (FDA) recently highlighted data integrity issues concerning premarket submissions received for medical devices. This was communicated in a Letter to Industry (medical devices) published by the agency on 20 February 2024.
Prior authorization is a formal process where a patient’s healthcare provider seeks approval from the patients health insurance company before proceeding with specific treatments, procedures, or medications. Patient Safety Prior authorization protects patients by: Verifying that prescribed medications or treatments are safe.
What is the best way for a medical sales rep to approach a medical professional in a hospital setting? What do nurses need to know if they want to consider medical sales as an alternative career? He is also extremely open to the possibility of nurses seeking opportunities in other spaces like medical sales. How are you?
The UK Medicines and Healthcare products Regulatory Agency (MHRA) has introduced new monthly safety bulletins aimed at making medical device and medicine safety information clearer and more accessible for healthcare professionals.
Pharmacists can educate patients about how to recognize unsafe online sources of medications and ensure patients are properly educate on how to administer their medications.
Auto-translations The ability to automatically convert content into other languages as needed, through domain-specific regulatory or safety language ontology sets is an important step in deploying automating IDP. Auto-translating streamlines communications purposes and drives efficiency gains.
While the product safety information page is among the top five pages visited what alarmed me was that time on the page was measured in seconds not minutes for most online visitors. Who could blame them when the safety information sounds like a medical journal? It doesn’t happen, and the FDA should know this by now.
In many European countries physicians can now prescribe medical cannabis for an array of chronic health conditions, including chronic pain, mental health disorders and neurological conditions. 1 In many countries, medical cannabis is only utilised as a therapy when licensed medications have proven ineffective. Just an excuse?
AI algorithms can analyze medical images and identify any abnormalities that may indicate cancer. In a study conducted by Korean academic hospitals and Lunit, a medical AI company specializing in developing AI solutions for radiology and oncology, the algorithm outperformed human radiologists in identifying breast cancer.
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