Medical Device Academy, Inc.’s Post

When you build(or buy!) a house, you make sure the foundations are in place before starting anything else. The same goes for starting a new medical device project. One of the major foundational pieces for starting a new medical device project is knowing (and following) the essential regulatory requirements ▶️from the beginning◀️. Ignoring or misunderstanding these requirements can lead to significant setbacks, financial penalties, and even project failure. Waddell Group wrote a blog article about it a while back. Today, I have broken the same article down into a 'quick read' pdf for everyone who doesn't have time to go through the entire article. To ensure early compliance with all the regulatory requirements, you need to do the following. Read it here⬇️

Is it a surprise that HCPs dislike filling out forms to download peer-reviewed scientific content, even if it's just their name and email? Probably not. Would it lead to drop-off? Yes, most likely. So why send out licenced ePrint content in a way that requires form filling when it can be avoided? To access published content, certain details like name and email are necessary. However, whether through email, at congress, or any other channel, the need to fill in a form can be removed by using Trustrack, offering HCPs a better experience with your brand, and achieving the best click-through rate as a result. Download our Trustrack flyer here (no form filling, we promise!) >> https://lnkd.in/gkgUAugQ

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One minute our Toothy is strolling through the park, the next he's balling at a billboard. He loves nothing more than a good Bronte, a powerful Keats, and a statistically significant reduction in a Phase 3 pivotal trial.   That's because words are Toothy's kryptonite. And they're at the heart of everything we do here at Word Monster | Powered by Medical Writing. They drive our medical affairs strategies, power our publications and energise our marketing propositions.   What words bring you to tears? Let us know your favourite quote or phrase and show us how powerful words are to you. Bonus points for anything #medcomms.

Navigating complex regulations in the medical industry can be overwhelming, but it doesn’t have to be! Our latest eBook, "The Medical Device Regulatory Survival Guide", breaks down the steps to streamline compliance with standards like ISO 13485 and 21 CFR regulations, helping you save time and focus on what matters—innovation and patient care. Check it out to learn how to simplify your processes and boost efficiency >> https://lnkd.in/eDNhmxR4

Unsure of how to begin your clinical trial? Look no further! The #CTToolkit is an interactive colour-coded routemap that provides guidance on legal and best practice requirements. Bursting with advice, it's a must-see for any aspiring researcher: https://lnkd.in/g8Epp7V

5 actionable tips to simplify medical content while keeping it engaging and empowering. These strategies will help you connect with your patient on a deeper level. Let's not confuse patients! #MedicalWriting #PatientEducation #PlainLanguage

📋 𝗦𝗶𝗺𝗽𝗹𝗶𝗳𝘆 𝘆𝗼𝘂𝗿 𝘀𝘆𝘀𝘁𝗲𝗺𝗮𝘁𝗶𝗰 𝗹𝗶𝘁𝗲𝗿𝗮𝘁𝘂𝗿𝗲 𝗿𝗲𝘃𝗶𝗲𝘄𝘀 𝘄𝗶𝘁𝗵 𝗼𝘂𝗿 𝗳𝗿𝗲𝗲 𝘁𝗲𝗺𝗽𝗹𝗮𝘁𝗲 Starting your literature review doesn’t have to be overwhelming. With Lindexer’s Literature Review Protocol Template, you can kick off your review process with confidence and efficiency. Designed specifically for medical devices and IVDs, this comprehensive resource helps you stay MDR-compliant while saving valuable time. 💡 𝗪𝗵𝘆 𝗶𝘁’𝘀 𝗽𝗲𝗿𝗳𝗲𝗰𝘁 𝗳𝗼𝗿 𝘆𝗼𝘂: 𝗦𝘁𝗿𝘂𝗰𝘁𝘂𝗿𝗲𝗱 𝗙𝗿𝗮𝗺𝗲𝘄𝗼𝗿𝗸: Pre-built sections guide you through every step. 𝗘𝗮𝘀𝘆 𝗖𝘂𝘀𝘁𝗼𝗺𝗶𝘇𝗮𝘁𝗶𝗼𝗻: Tailor it to fit your unique project needs. 𝗧𝗶𝗺𝗲-𝗦𝗮𝘃𝗶𝗻𝗴: Spend less time planning and more time analyzing. ✅ 𝗪𝗵𝗼 𝗶𝘀 𝗶𝘁 𝗳𝗼𝗿? Researchers, medical writers, and professionals looking to simplify their workflows and deliver high-quality, compliant reviews. 🔗 Download it for free and start streamlining your process today: https://loom.ly/2HQO1Go #Lindexer #LiteratureReview #MedicalDevices #SystematicReview #MedWriting #ResearchTools

Are you tired of getting newsletters in your inbox that are long, drawn out, or irrelevant? At in2being, we're committed to carefully crafting our newsletters to be brief, helpful, and straight to the point so you get the information you need to stay confidently in the know about medical device development. They're sent out less than once a week, and signing up is easy and takes only a few seconds. You won't regret it. Your inbox won't, either. https://lnkd.in/gYbYFjfP

IMPROVING PATIENT CONFIDENCE Could your patients benefit from visual aids to help them navigate medical devices or better prepare for procedures? Let’s collaborate to create clear and engaging content that enhances their understanding and confidence. Reach out to explore how we can help!