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Product Development & Innovation

R&D department is responsible for conceptualizing, designing, and developing new medical devices. Innovation is often driven by clinical needs, technological advancements, and regulatory changes. R&D teams aim to develop devices that enhance patient outcomes, improve diagnostic accuracy, and streamline healthcare procedures.
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Regulatory Compliance and Standards

Medical devices must comply with strict regulatory standards like IMDR 2017 (India), FDA (USA), and MDR EU 2017/745 (Europe). The R&D department ensures compliance through documentation, clinical testing, and safety validation.
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Materials
Research

In medical device manufacturing, materials are crucial for safety and performance. R&D teams focus on biocompatibility, ensuring materials are safe, non-toxic, and effective in medical environments. Extensive research is conducted to meet these standards.
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Prototyping &
Testing

Once a concept is developed, the R&D team creates prototypes to test the device's functionality, safety, and efficacy through rigorous testing in simulated clinical environments. Multiple iterations of prototyping and testing refine the device before production.
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Clinical Trials &
Validation

For high-risk medical devices, clinical trials are essential for regulatory approval. The R&D department oversees clinical validation, testing the device in real-world settings. This ensures the device meets safety, efficacy, and performance standards for market acceptance.
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Collaboration with Healthcare Professionals

Close collaboration with doctors, surgeons, OT technicians, and other healthcare professionals is crucial for the R&D department. Their feedback on practical use, ergonomic design, and patient care helps refine the device. This ensures the final product meets clinical needs and improves healthcare delivery.
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R&D

Research & Development

Advancing Innovation
in Medical Technology

Plays a pivotal role in driving innovation and ensuring the development of safe, effective, and cutting-edge medical technologies. We mainly focus on research, regulatory compliance, and continuous improvement to meet the needs of healthcare providers and patients.

Work Flow of r&D

Requirments

Analysis

Generating ideas

Resource Mobilization

Concept Development

Theoretical designing

Prototype

Testing

Feed back

Production

Trends and future
of our staan R&D

Minimally Invasive Technologies: There is a growing emphasis on developing devices for minimally invasive procedures, such as advanced endoscopic tools, catheter-based systems, and robotic surgery devices. These innovations are aimed at reducing recovery time and improving patient outcomes.

Sustainability: sustainability is becoming a priority. Medical device R&D is exploring ways to reduce the environmental impact of devices through more sustainable materials, reducing energy consumption during production, and improving recyclability

R&D department in STAAN is a cornerstone of innovation, responsible for the development of new devices that improve patient outcomes while navigating complex regulatory landscapes. With the integration of new technologies and a focus on personalized, connected healthcare, the future of medical device R&D holds tremendous potential.

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