Vast Experience in MedTech
Leading international manufacturers of medical products entrust us with their communication and digital projects. Taking a holistic approach, we create individual and complete solutions just the way you envisage them. We also optimize and automate processes to save time and to cut costs.
MedTech Areas Where We Have Particular Expertise
Technical Communication
Working together with various departments at your company, we help you to reach your time-to-market objectives by producing surgical techniques, (electronic) instructions for use (IFU), case studies, manuals, websites and a host of other products in accordance with regulatory standards.
Marketing Communication
You have an array of different stakeholders – from surgeons or purchasing agents to conference participants or patients – and you communicate with them through a variety of channels. We design the ideal advertising for you: stand articles for trade shows and giveaways for your perfect appearance at a conference, eye-catchers for successful product launches or fliers and a website on your products to provide straightforward information.
MDR
With the ongoing changes to the Medical Device Regulation (MDR), you must constantly revise your communications and we are happy to help you with that task.
GXP/CSV (Good Documentation Practice/Computer Systems Validation)
We assist you in defining your processes and in validating your computer systems to ensure your compliance with the regulations imposed by the FDA, Swissmedic, ISO 9001, ISO 13485 and others. We gladly advise you on implementation and define the necessary interfaces together with you. All the while, we guarantee you discretion and protect your data and business interests.
Our Services
- Consulting and Project Management
- Technical Communication
- Marketing Communication
- Contracting
- MDR/IVDR
- Proofreading and Editing
- Photo Shoots and Image Processing
- DAM Solutions
- Multi-Channel Publishing
- Printing Solutions
While adjusting to the new EU regulation, you can boost efficiency in vital ways. Stämpfli Communication is here to help you do just that.
The ever-greater regimentation of the medical technology industry demands much of companies in this sector. They must expend increasing amounts of time and resources just to keep up to date.
With the replacement of the Medical Device Directive (MDD) with the Medical Device Regulation (MDR) of the European Union, the binding rules on the manufacture and marketing of medical products have become all the stricter. Corrective and preventive measures are also needed on an ongoing basis, as part of internal quality control or as a result of complaints filed by the TÜV or the FDA.
In any event, Stämpfli Communication is here to guide you through the adjustment process to make certain that your communication materials are in conformity at all times.
Do you lack the internal resources to implement MDR projects on time? We provide you with resources and help to overcome any bottlenecks. Drawing on our wealth of industry-specific experience, we connect quickly with your people, be they consultants, project managers or specialized personnel in charge of implementation. We help you to tackle concrete challenges and to reach key objectives. From our facility in Bern or on-site integrated in your company.
