Racer’s mechanical engineering services can help you to transform ideas to manufacturability products by developing guidance models, and graphics for manufacturing process. Our mechanical design team uses the state-of-the-art tools and follow the industries’ best practices to ensure excellent manufacturing outcomes. Navigating the journey from concept to commercialization for medical devices is a multifaceted process that demands precision, expertise, and regulatory compliance.

It’s a dynamic journey where collaboration, innovation, and adherence to quality standards are paramount. Partnering with us gives you access to our resources which can be a true engineering extension of your company. With the help of our facility’s pre-engineering tools and years of experiences building products, we are able to turn your products into reality.

We carefully review and inspect your designs, and make efficient improvement & optimization on the DFM to meet the customer’s satisfaction. This doesn’t only provide our customers the opportunity to build the most reliable but also at the most reasonable and cost-effective product without compromising your original idea.

We practice such tool to select the most cost effective material and process to be used in the production of early stage product design. We minimize part count and design parts by adding self-locating features. This can minimize orientation and also advocate modular design. 

Racer has the tool, knowledge and experience in PCBA design that can function according to your project needs. Despite of all the sophisticated technical issues, size or design defects that might be encountered by our customer. Our customers can provide their concept or idea, and Racer team will support it from conception to completion. Experience this one-stop PCB solution with our well-known and certified partners with various production capabilities.

We navigate the complex landscape of regulations to facilitate smooth approvals and market entry.

Ensuring regulatory compliance is a cornerstone of our commitment to delivering safe consumer-used electronic devices under our care. Navigating the intricate landscape of regulations (e.g., Consumer safety, Waterproof, Electrical Safety), our dedicated team meticulously adheres to stringent standards set by regulatory authorities. From initial concept to commercialisation, every phase of the product lifecycle is guided by a comprehensive understanding of regional and international regulatory requirements. Rigorous testing, documentation, and quality control processes are implemented to meet or exceed these standards, guaranteeing the safety, efficacy, and reliability of our medical devices. By prioritising regulatory compliance, we not only meet legal obligations but also underscore our unwavering dedication to the well-being of the end-users. 

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