Medical Devices

No matter if we are talking about non-active or active medical devices, in vitro diagnostic medical devices (IVDs) or medical device software, we can support you along the way. The classification of your "borderline products" is also in good hands with our specialists.

knoell Medical Devices

fast and successful access to your key markets

As an independent globally operating consultancy, knoell's international team of more than 20 medical device experts includes specialists in biomedical engineering, software engineering, medical sciences and medical writing, pharmacology, toxicology, chemistry and biochemistry.

We support manufacturers of medical devices and in-vitro diagnostic medical devices (IVDs) with our extensive expertise at every point of the product life cycle. Our medical device experts support you in gaining access to global key markets like Europe, North & South America and Asia.

Together with our clients we build a sound market access strategy by identifying the most efficient route to place your products on the desired market.

 

Contact for Europe, Asia & the USA                                     Contact for South America
Photo of Dr med. Isabelle Lang-Zwosta
Dr med. Isabelle Lang-Zwosta
Maik Endler_Managing Director
Maik Endler

Learn more about implementation strategies for IVDR with our e-Learning series!

In a series of 9 sessions we will help you to understand how the new IVDR will affect your product. Topics covered by our IVDR learning videos:

Our Medical Devices solutions for you

No need to invest your valuable time to keep the project moving: our experienced project managers will assure that your project runs smoothly, no matter if we are talking about total outsourcing or just a smaller task within the submission process. This is how it could look like for you.

Authorities in most markets require medical device companies to maintain a quality management system to obtain device approvals and registrations. We implement and maintain quality management systems (QMS) that comply with QMS regulations in medical device markets.

  • QMS - implementation / maintenance (e.g. ISO 13485, 21 CFR 820, RDC 16)
  • MDSAP - implementation
  • CAPA - support
  • QMS - interim management
  • Auditing - internal / supplier (on-site / remote)

Read more about our quality management and audit solutions for you.

From proof of concept to developing a sound design & product safety plan. We support you along the way. Non-active, active or software: find more details on our medical device design & development support here.

Explore how knoell can support you with your clinical and biological safety tasks.

Knowing your regulatory environment is essential to stay in the market and to grow your business. With our global network of affiliates, knoell keeps track of the developments concerning global regulations for medical devices and IVDs.

Our team supports with

Read more about our strategic and regulatory consulting solutions.

Optimise the way you perform your day-to-day work. Automation can help.

Benefit from our up-to-date expert training modules, seminars and workshops held on scheduled dates at our training premises, online or at a location of your choice and individually designed for you. Explore our knoell academy programme!

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Latest News & Events on Medical Devices

spalten3

Chemical Watch Expo 2020

09 - 11 dez 2020
online event
Moved online

COMPAMED 2020

16 - 19 nov 2020
online event

Innovationstage Medizintechnik

10 - 13 nov 2020
online event