The Berlin-based consultancy BEO BERLIN will be represented with a stand at this year's REHACARE (Hall 4 / E03). This year, the company is offering extensive points of contact for manufacturers in the homecare sector with experts on key days.
1. Focus day HMV & DiGA "Day of the solution for listing issues" on Wednesday, 14 September 2022
The experts offer visitors information on the topic of "medical aid number" and "DiGA". Manufacturers of medical devices can expect to learn more about the differences between DiGA and medical aids during on-site discussions, starting with assistance with classification.
Interested parties receive tips from over 20 years of experience in the market: How can my product be included in the list of medical aids? What tasks need to be solved? What hurdles are to be expected?
2. Focus day "Quality management for manufacturers of medical devices" on Thursday, 15 September 2022
On site, experts offer information on the topic of "Quality management for manufacturers of medical devices"The BEO BERLIN® team will discuss with visitors what requirements exist, especially for manufacturers of Class I products. What is the scope of a QM system for your company? How do I avoid changes to existing functioning processes in the company and still remain or become MDR-compliant? What potential for improvement is there for less good processes?
3. Focus day "MDR and requirements for start-ups" on Friday , 16.09.2022
New innovative companies in particular, i.e. start-ups, are confronted with many regulatory hurdles for the first time. However, these should not slow down your energy. As Medical Device Consultants at BEO BERLIN, we provide guidance and practical information on the topic of "MDR and requirements for start-ups". Experts will discuss with you on site when is the right time to start CE documentation. What do you do yourself and what do you give out? What else needs to be considered in addition to the MDR and what comes after CE certification? Frequently asked questions are answered: How do I combine my idea with other (medical) products? When do I contact the notified body? What about the classification, or is it really a medical device and what does that mean for me as the responsible person?
BEO BERLIN is a constant and reliable partner when it comes to implementing the requirements of the MDR and the many changes in the field of medical aids. Visitors and exhibitors are welcome to address their questions regarding the innovations in the market to the experts of the Berlin-based company on site in Düsseldorf.
Free consultation appointments at the trade fair with the Medical Device Consultants at the company stand (Hall 4 / E03) can be arranged by telephone or contact .
