What we do
We support emerging MedTech companies with their clinical trial needs in obtaining and maintaining device market approval. Based on our experience since 1988 we will come up with a smart solution to get your device on the market and keeping it there as safely, effectively and affordably as possible. We like to keep things simple, with our ISO13485 certification we ensure that we never lose sight of quality. We work with start-up companies initiating first-in-man studies, to more emerging companies focusing on their post-market clinical follow-up activities.
Our services are divided into four pillars:
Our mission
Our mission is to build balanced partnerships with clients to navigate emerging med-tech products throughout the market approval lifecycle.
Our vision
Cooperating with Bevinced provides a trusted partnership; you are the expert in all aspects related to your product, Bevinced is the expert in obtaining and maintaining market approval for med-tech. We believe collaboration and transparency are crucial to bringing our project to a successful conclusion.
Our mission
Our mission is to support the medical device industry in providing safe and effective MedTech solutions. We are dedicated to keeping as many medical devices on the market as possible and to maximize device accessibility by offering high-quality and cost-effective clinical trials and regulatory services.
Our vision
In a nutshell, the Medical Device Regulation (MDR) is designed to emphasize safety throughout the medical device lifecycle. We encourage this purpose, as long as manufacturers are not hampered by the high demands, and device market access and accessibility is not impacted.
Therefore, we are committed to effective planning, operation and control of processes to meet applicable standards, guidelines and regulations.
We understand manufacturers face high costs when getting medical devices to market, and we see these costs increasing due to MDR requirements. As such we consciously and efficiently organize our services in terms of time, budget and resources. Every day counts in getting medical devices to market or keeping them there; hence we strive for fast turnaround in everything we do.
Our Values
We focus on our core strengths:
Transparency
It's our core practice to act transparent and trustworthy, and we expect our clients to do the same. We believe honesty is the backbone of our collaboration; only when we know all relevant facts can we build a joint customized solution to deliver the project successfully.
Promise to clients
We stay true to the words we speak. We understand high costs come with market approval, hence we consciously and efficiently organize projects in terms of time, budget, and resources. Every day counts in getting your product to market; hence we strive for fast turnaround in everything we do.
Quality
We focus on small details while never losing sight of the bigger scheme. We ensure effective planning, operation and control of processes to meet applicable regulatory requirements, standards and guidelines. Quality for us means maintaining the highest quality standards and striving to meet expectations in all we do.
Our team
Dirk Meijer
Joris Bannenberg
Pascal Groenen
Marloes van Laarhoven
Anne Pauline van der Wilden-van Huijstee
Francine Mathot
Lisa Heeremans
Federica Spiga
We are a growing company, always looking for talent.
Do you want to be involved in all aspects that come with obtaining and maintaining market approval in the MedTech industry? And are you excited to support the growth story of our company? Join our team!