Schlafender Hase

Why Adherence to Medical Device Labeling Standards is Essential 👇 Labeling standards in the medical device sector are more than just guidelines—they are critical to patient safety and regulatory compliance. 1. Regulatory Compliance is crucial, as incorrect or misleading labeling can compromise patient safety and lead to costly recalls. 2. Legal responsibilities pertain to compliance with regulatory standards, accurately represent the device's specifications and usage, and are updated to reflect any changes. 3. You enhance patient safety by ensuring error-free and thorough instructions on proper use, handling, and risks. 4. Medical device labeling training provides essential information for users regarding appropriate use, handling, and potential risks. 5. Medical device traceability is vital. The FDA and EU require Unique Device Identifier (UDI) compliance on some classes of medical devices. Get the Medical Device Label Management Compliance Guide at the link in the comment section. #MedicalDevices #PatientSafety #RegulatoryCompliance #Labeling

The future of product labeling is here, and it's powered by FHIR (Fast Healthcare Interoperability Resources). After moving into electronic submissions with SPL, we’re now embracing the age of #FHIR. So, what does this mean for the industry? Here are the key benefits: - Cost and time efficiencies through better information exchange - Greater potential for scalability - Risk mitigation by automating workflows and processes—no manual transposition or replication needed - Empowering patients, physicians, and stakeholders with more accessible information - Seamless information exchange across various devices and media Read the Full article "FHIR: Transforming Product Labeling" at the link in the comment section.

How are suppliers coping with the medical device sector’s surging regulatory burden? Life Sciences Voice asks Peter Muller & Mike Baird of Schlafender Hase here https://bit.ly/4h9Uve3. With reference to new research, they are considering how well Class 2 and 3 device manufacturers are adapting. #medicaldevice #regulatoryrequirements #elabelling #FHIR

We had a great time at the Future of Pharma Marketing Summit! We even had a surprise guest; wonderful seeing you Abhishek MK 😀 Thank you Pharma Marketing Canada for a well-organized event!

Day 2 at Future of Pharma Marketing Summit 2024 is underway! 🐰 If you haven’t stopped by yet, hop on over and grab one of these little guys! #FuturePharmaMarketing2024 #PharmaMarketing 

Attending the 6th Annual Future of Pharma Marketing Summit 2024 by Pharma Marketing Canada? Come take a selfie with the Rabbit! If you post it and tag us, you will be entered in to win a 150$ Amazon Card! #FuturePharmaMarketing2024 #PharmaMarketing #HealthcareMarketing

Join Peter Muller & Vineed Ravindranath for a quick 20-min LinkedIn Live session on the evolving medical device sector! 🩺 We'll cover top opportunities, challenges, and tips to stay compliant in this fast-evolving space.

Join Us Tomorrow for an Insightful Discussion! 👌 Join Peter Muller and Vineed Ravindranath as they dive deep into this evolving landscape, highlighting the opportunities for innovation, the challenges that come with increased compliance, and the strategies you can adopt to stay ahead. #MedicalDevices #RegulatoryCompliance 

If you are attending #CAPRA2024 today, don’t miss the chance to connect with Peter Muller and Tara Warner to learn how TVT can bring peace of mind to your regulatory processes. CAPRA - Canadian Association of Professionals in Regulatory Affairs

Do you know what Schlafender Hase means? Come meet Peter Muller tomorrow at the 6th Annual Future of Pharma Marketing Summit 2024 to find out 😉 Pharma Marketing Canada #FuturePharmaMarketing2024 #PharmaMarketing #HealthcareMarketing