ABOUT
At Hands on Research, our secret sauce is our team of experts who are highly experienced in the medical device industry and have a proven experience of regulatory compliance and clinical evaluation. Our team includes scientists, engineers, regulatory affairs professionals, and clinical research experts who work together to provide a comprehensive approach to product development and regulatory approval.
We have a track record of success in helping our clients bring their medical devices to market quickly and efficiently while ensuring regulatory compliance and patient safety. Our team is committed to staying up-to-date on the latest regulatory requirements and industry trends, and we work closely with our clients to develop customised strategies that meet their specific needs.
We also have a strong focus on quality and customer service. We understand that navigating the regulatory process can be challenging, and we strive to provide our clients with the support and guidance they need to succeed. We are always available to answer questions, provide updates, and ensure that our clients are fully informed throughout the regulatory approval process.

REGULATORY CONSULTANCY
Our team of experts will advise you on regulatory strategies, help you prepare and submit regulatory applications, and provide ongoing support throughout the approval process. We are familiar with the regulatory requirements of major markets around the world, including the US, Europe, and Asia.
We pride ourselves on our commitment to quality and customer service. Our dedicated team will help you achieve your regulatory and clinical goals, and we are always available to answer your questions and provide support when needed. Contact us today to learn more about our services and how we can help you bring your medical devices to market.
Why choose us?
Expertise
Our team of experts has extensive knowledge and experience in regulatory affairs, clinical evaluation, biocompatibility testing, post-market surveillance, and other areas of medical device consulting. We stay up-to-date with the latest regulations and guidance, and we use our expertise to help our clients navigate complex regulatory requirements and achieve their goals.
Quality
We are committed to providing high-quality, reliable services that meet the needs of our clients. We have a rigorous quality management system in place that ensures that our work is accurate, thorough, and compliant with relevant regulations and standards.
Customised Solutions
We understand that every client and every device is unique, which is why we offer customised solutions that are tailored to the specific needs of each client. We work closely with our clients to understand their goals, challenges, and constraints, and we develop solutions that meet their needs and exceed their expectations.
Cost-effective
We offer competitive pricing and cost-effective solutions that help our clients achieve their goals while staying within their budgets. We are committed to providing value to our clients and helping them achieve their goals in the most efficient and cost-effective way possible.
Partnership
We believe in building long-term partnerships with our clients based on trust, collaboration, and mutual respect. We are committed to working closely with our clients to achieve their goals and help them succeed in the competitive medical device market.