Schlafender Hase

Schlafender Hase is proud to be a sponsor at the Future of Pharma Marketing Summit 2024! 🚀 Peter Muller and Tara Warner are looking forward to connecting with industry leaders and exploring the latest challenges and opportunities in pharma marketing. #FuturePharmaMarketing2024 #PharmaMarketing #HealthcareMarketing

Join Peter Muller & Vineed Ravindranath for an engaging 20-minute LinkedIn Live! We'll explore the latest trends shaping the medical device sector—uncovering top opportunities for innovation and addressing the key challenges impacting the industry. Plus, get actionable tips to help you navigate regulatory compliance in this rapidly evolving landscape. Join us here 👇

We’re thrilled to highlight “ePI is on FHIR Around the Globe”, bringing together top innovators from Europe, Asia, and the Middle East. Join this virtual event to discover how FHIR technology is transforming electronic Product Information (ePI). Get inspired by real-world success stories and cutting-edge digital health solutions driving the future of patient care! 👇

Adapting to Increasing Regulations in the Medical Device Industry: Key Strategies 💪 In the face of growing regulatory demands, how are medical device companies adapting? A 2024 study commissioned by Schlafender Hase surveyed 202 regulatory professionals at Class 2 and 3 medical device companies in Germany and the US to find out. Here are the top five strategies respondents are using to manage the impact of increasing regulations: - Implementing Key Standards/Controls (e.g., ISO standards) – 37% of respondents are taking this approach, with the figure rising to 41% among EU (German) companies. - Process Automation – Also cited by 37%, this strategy is particularly prevalent in Germany and the EU, where over 40% of companies are automating processes. - Process Digitization – 33% of respondents are digitizing processes to stay compliant. - Increased Outsourcing/3rd Party Collaboration – 33% are turning to external partners to manage the regulatory load. - Hiring More Regulatory Professionals – 32% are expanding their teams to keep up with the demands. As regulations continue to evolve, it's clear that a combination of standards implementation, automation, digitization, and strategic partnerships is key to staying compliant and competitive. How is your organization responding to these challenges? Download the report here: https://lnkd.in/ekyjKSXT #RegulatoryAffairs #MedicalDevices #Compliance

Boosting Labeling Accuracy to 99% with TVT 🙌 In industries where precision is paramount, ensuring the accuracy of labels is crucial. Mistakes in labeling can lead to severe consequences, from regulatory fines to compromised consumer safety. This is where TVT comes in, revolutionizing the way companies handle label verification and boosting accuracy rates. Steve Pollock, a Graphic Specialist/R&D Systems Administrator, shared his experience with TVT: "Since using TVT, I can say that about 99% of our labels are correct. In an industry where accuracy is everything, this is significant for our company."

Are you an experienced Project Manager with an entrepreneurial spirit and an analytical mindset? Join our team at Schlafender Hase and lead the implementation of strategic business development projects that will expand our global market presence. This is an exciting opportunity to work with our international team and make a real impact! Location: Frankfurt am Main, Germany Position: Permanent, Full-time Ready to take on this challenge? Learn more and apply here: https://lnkd.in/e37_R24V

Pharmaceutical companies are tasked with navigating highly regulated environments that demand accuracy, speed, and compliance. Structured Product Labeling (SPL) plays a critical role in ensuring that product information is communicated consistently and clearly across the industry. LexisNexis Reed Tech and Schlafender Hase provide innovative solutions to these challenges. With over 20 years of experience, Reed Tech leads in SPL preparation, submission, and lifecycle management. Schlafender Hase’s TVT, ensures error-free and compliant packaging, enabling pharmaceutical companies to streamline their labeling processes while adhering to FDA and EMA standards. See how our partnership is helping pharmaceutical companies meet regulatory demands head-on. Read the case study at the link in the comment section. #Pharmaceuticals #RegulatoryCompliance #SPL #Labeling

Join Peter Muller & Jamie Reid for an engaging 20-minute LinkedIn Live session where we'll explore the latest trends shaping the medical device sector! 🩺 We'll dive into the top opportunities for innovation, the pressing challenges impacting the industry, and provide actionable tips to help you navigate regulatory compliance in this rapidly evolving landscape. Join us here: https://lnkd.in/e8EtJ72P

Feeling frustrated with proofreading multilingual documents? You're not alone. With the capability to spell check multilingual documents, TVT ensures accuracy whether your team speaks the language or not. Featuring 48 dictionaries, including Arabic, Hebrew, and Thai, TVT Spelling can seamlessly check multiple files with various formats and layouts in a single review session. Streamline your multilingual document comparison process with TVT today. Learn more 🔗https://lnkd.in/e2NJyWe7

Find out what Peter Muller & Mike Baird of Schlafender Hase think about how Class 2 and 3 medical device manufacturers in Europe and the US are adapting to soaring regulatory demands here https://bit.ly/47MwHs9 in International Pharmaceutical Industry Journal #medicaldevice #regulatoryrequirements #elabelling #FHIR