Clinical Stakeholder Engagement: How Building Trust Today Fuels Growth Tomorrow
At every stage of medical device development, engaging relevant clinical stakeholders is essential for product success. If you
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Crossing the Chasm: Affordable Solutions for Medical Device Innovation
Innovation in medical devices is vital to advancing healthcare, yet the journey from concept to market adoption remains
Understanding FDA Pre-Submissions
The FDA Pre-Submission (pre-sub) program is a game-changer for medtech and pharma companies. It allows you to get
Podcast: “Clinical Evidence, The Key to Market Adoptions”
Market access strategies for medical devices In the latest Global Medical Device podcast episode, Etienne Nichols is joined
RLS presents at BioTech Breakfast during New York Tech Week
Phase Capital and 615.vc hosted a dynamic BioTech Breakfast as part of New York TECH WEEK by a16z,
Regulatory approval is just the beginning of your medical device journey
Attention MedTech Innovators and Entrepreneurs Regulatory approval is just the beginning of your journey to market success!
3 Quick Tips to Nail that Clinical Study the First Time
Clinical data is the gateway to achieving market access and market adoption for medical device and drug innovations.
Commericalization GPS
Envision taking a road trip to an unfamiliar state, navigating solely by your instincts and without a GPS.
Medical Device Commercial Path
Launching a medical device in the next 1-3 years? Seeking funding for your medtech startup? Investing in a
Lesson I Learned About Clinical Research
“I don’t trust people who have never failed at something.” That’s what my friend said yesterday, and I
What Medical Device Companies Should Know about the MDR Extension – It’s Time!
The European Union (EU) adopted the Commission’s proposal to extend the Medical Device Regulation (MDR). The amendment was
Is it Okay to Copy a Clinical Design?
I’m considering using a similar study design from another company to expedite the regulatory clearance process for my
