Operating in Sweden requires strict adherence to the Läkemedelsverket (Medical Products Agency) and EU-wide GDPR standards. Our solutions integrate "Privacy by Design," ensuring patient data remains encrypted and sovereign.
Sweden’s high digital literacy and BankID infrastructure provide a unique advantage. Our DCT platforms are designed to integrate seamlessly with 1177 Vårdguiden and regional electronic health records (EHR).
Our factory is not just a production line; it is a center of innovation. We provide tailored decentralized clinical trial solutions, from customized wearable biosensors to branded patient engagement apps, specifically designed for the Swedish demographic.
With streamlined export processes and strategic partnerships with global logistics leaders, we ensure that clinical kits, diagnostic reagents, and hardware reach Swedish research centers in Stockholm, Gothenburg, and Lund with minimal lead times.
Dongguan Trial Medical Co., Ltd. is a specialized manufacturer of remote clinical trial monitoring devices, decentralized clinical trial solutions, and digital research technologies. Established in 2016, the company is located in Dongguan, China, a major center for advanced manufacturing, medical technology development, and electronic innovation.
Operating from a modern facility covering more than 11,000 square meters, with a team of over 230 employees, Trial Medical is dedicated to developing and manufacturing innovative technologies that support clinical research organizations, pharmaceutical companies, healthcare institutions, and academic research centers worldwide.
The company's product portfolio includes remote clinical trial monitoring devices, wearable health data collection systems, patient engagement platforms, electronic clinical outcome assessment solutions, digital research tools, remote safety monitoring systems, and decentralized trial support technologies. These solutions are designed to facilitate real-time data collection, improve participant engagement, streamline study management, and enhance operational efficiency throughout the clinical research process.
Implementing algorithms that can predict patient non-compliance or adverse events before they occur by analyzing real-time data streams from wearable devices.
Creating immutable audit trails for clinical data to satisfy the most stringent EMA (European Medicines Agency) inspections and ensure 100% reliability.
Reducing the carbon footprint of clinical trials through eco-friendly packaging and recyclable diagnostic components, aligning with Sweden's environmental goals.
A: All our digital solutions are built to be GDPR compliant. We offer localized server hosting options within the EU and employ end-to-end encryption for all patient-generated health data (PGHD).
A: Yes, we specialize in OEM and ODM services. We can customize hardware, firmware, and software interfaces to meet the specific protocols of your clinical study.
A: Standard orders are processed within 7-14 days, with air-freight delivery to major Swedish hubs taking an additional 5-7 business days, depending on customs clearance.
A: Absolutely. Our facility is ISO 13485 certified for medical device manufacturing, ensuring the highest level of quality and reliability for clinical applications.
Contact our expert team today to discuss your decentralized trial requirements, OEM needs, or supply chain optimizations.
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Trial Medical
