Generating viable ideas from diverse sources and teasing out winners is the first step on the journey to a successful launch. We provide qualitative and quantitative research / analytics to decide where to invest.
This may include assembling multiple stakeholder advisory boards, in-depth customer interviews and online surveys.
We've helpe
Generating viable ideas from diverse sources and teasing out winners is the first step on the journey to a successful launch. We provide qualitative and quantitative research / analytics to decide where to invest.
This may include assembling multiple stakeholder advisory boards, in-depth customer interviews and online surveys.
We've helped start-ups co-create with clinical leaders and multinationals work though a product ideas backlog hundreds of line items long while building a transparent system for collecting, aggregating, and reviewing future ideas.
To write effective product requirements, product management must translate between the market and engineers. At Veralur, we've developed dozens of products of all different categories and applications in MedTech. Many of these remain best-in-class years after launch without a single recall or remediation.
In addition, we offer a network o
To write effective product requirements, product management must translate between the market and engineers. At Veralur, we've developed dozens of products of all different categories and applications in MedTech. Many of these remain best-in-class years after launch without a single recall or remediation.
In addition, we offer a network of design house and contract manufacturing partners to execute Design History File based development. Veralur can guide this process, recommending tradeoff decisions and ensuring budgets and timelines are met.
We can help find the best regulatory path based on your technology, clinical application, patient groups, etc. Once on your way, gathering feedback and iterating on protoypes is not just potentially a regulatory requirement (usability, human factors), but also a great way to ensure users will want to keep engaging with your solution over
We can help find the best regulatory path based on your technology, clinical application, patient groups, etc. Once on your way, gathering feedback and iterating on protoypes is not just potentially a regulatory requirement (usability, human factors), but also a great way to ensure users will want to keep engaging with your solution over time.
We can guide and execute this formal process for you along with solution validation against the original requirements for Design History File documentation and commercialization claims purposes.
Preparing for an impactful launch is key to making your investment count and gaining traction before competition does.
Veralur knows how to make a winning first impression with customers whether its online, on the tradeshow floor or in the operating room. Over twenty years, we've launched dozens of products, services, subscriptions and in
Preparing for an impactful launch is key to making your investment count and gaining traction before competition does.
Veralur knows how to make a winning first impression with customers whether its online, on the tradeshow floor or in the operating room. Over twenty years, we've launched dozens of products, services, subscriptions and integrated solutions.
Do you have a solution that's underperforming post-commercialization? Let us diagnose why and re-launch to meet your goals! Read our case study here.
Kristin Wagner, Veralur's Principle & Owner
Boston, Massachusetts, United States
Veralur MedTech Consulting
Boston, Massachusetts, United States
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