Our Expertise
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Concept Development & Feasibility Studies
We help translate your vision into a tangible concept, conducting thorough feasibility studies to assess its technical and commercial viability.
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Design & Engineering
Our multidisciplinary team of engineers excels in designing and developing a wide range of medical devices, from minimally invasive surgical instruments to sophisticated diagnostic systems.
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Prototyping & Testing
We rapidly prototype your device using state-of-the-art technologies and conduct rigorous testing to ensure safety, efficacy, and compliance with regulatory standards.
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Manufacturing & Commercialization
We guide you through the entire manufacturing process, from selecting the optimal manufacturing partners to navigating the complexities of regulatory approvals and market entry strategies.
Our Commitment
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User-Centered Design
We prioritize patient needs and safety in every stage of the development process.
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Quality & Compliance
We adhere to the highest quality standards and ensure compliance with all relevant regulatory requirements (e.g., FDA, CE Mark).
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Innovation & Collaboration
We foster a culture of innovation and collaborate closely with our clients to achieve shared goals.
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Confidentiality & Integrity
We maintain the utmost confidentiality and integrity in all our engagements.
Let's Partner to Improve Healthcare:
Whether you have a groundbreaking medical device concept or need assistance with a specific development challenge, Vasmed is your trusted partner. Contact us today to discuss your project and learn how we can help you bring your innovative medical solutions to market. Let us help you navigate the complexities of medical device product development and bring your ideas to life.
We can build a sample proof of concept for your idea prior to any project commitment.*
*T&C apply
Product Development capabilities
At Vasmed, we are dedicated to transforming innovative ideas into high-quality medical devices that improve patient outcomes and meet the demands of healthcare professionals. With extensive experience in medical device design, engineering, and regulatory compliance, we offer end-to-end solutions to bring your vision to life from concept to commercialization.
Our Expertise in
Medical Device Development
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Conceptualization and Design
Our product development process begins with understanding our partners unique needs. Our multidisciplinary team of engineers, designers, and clinicians works collaboratively to create device concepts that are not only functional but also user-friendly. Whether you're developing an active diagnostic tool, therapeutic device, or invasive surgical medical device, we focus on designing safe, effective products that align with relevant medical regulatory standards.
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Prototyping and Testing
Once the design concept is finalized, we quickly move to prototype development, utilizing advanced technologies such as 3D printing, rapid prototyping, and simulation, using our platform PCBAs and software we have a very short turn-around time for prototyping, to show the proof of concept on the concept devices.
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Engineering and Development
Our engineering team leverages cutting-edge technologies and materials to refine the design and address any technical challenges. Our standardised product realisation process is compliant to ISO 13485:2016 requirements and ensure adherence to all the documentation being released at various stages of the product development, to meet with the regulatory compliances of MDR, FDA and other country regulatory requirements, with minimal additional documentation efforts.
We specialize in a wide range of medical device types, including Active critical care devices, Class III PTCA Catheters, Class III PTCA guidewires, Invasive blood pressure monitoring systems, wearable devices, implantables (transient and long-term), and diagnostic tools. We ensure that every product is built with scalability, cost-effectiveness, and ease of manufacturing in mind, while maintaining the highest level of precision and performance.
Our Master deliverable list, ensure compliance with various regulatory requirements including ISO 13485, MDR, and FDA requirements. Our project development process allows for flexibility to adapt to customer documentation templates so that it can be included in the product development process from the beginning of the project to ensure compliance to customer quality management systems at the certification stage of the project.
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Regulatory Affairs and Compliance
Navigating the regulatory landscape is a critical part of medical device development. We provide comprehensive support through the complex processes of FDA approval, CE marking, and other international regulatory requirements. Our team of regulatory experts ensures that your device adheres to all necessary guidelines, including ISO 13485, IEC 60601, and other relevant standards, so you can bring your product to market with confidence.
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Manufacturing and Quality Control
Our manufacturing solutions are designed to scale with your product’s lifecycle. We use state-of-the-art manufacturing techniques to produce medical devices with the highest precision and quality standards. Our quality control processes are robust and rigorous, ensuring that each product undergoes thorough inspection and testing to meet all performance and safety requirements.
Refer Manufacturing capabilities for details.
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Post-Market Support
After the product is launched, our team remains a trusted partner for post- market surveillance, product updates, and ongoing support. We assist in collecting feedback, monitoring product performance, and making enhancements to ensure long-term success in the market.
