With multiple project management teams and rich data management experience, Teddylab constantly adapts to changes in domestic and foreign regulations and customer needs.

Teddylab's senior professional team implements quality assurance in every aspect of clinical research, and provides full-process management services for registration and application. Teddylab's project operation officer has PMP certification and its department director has 15 years of experience in clinical trial projects management of central laboratory with a multi-level management team of PMs and PAs. We have more than 200 Asia-Pacific and domestic projects, trainings initiated by more than 30 sites for a single project at the same time, and senior project management experience for more than 20 different testing systems for a single project. We provide you with project initiation, management and tracking services throughout the process.

Our comprehensive and complete document management system can provide you with personalized customization and preparation of project operation documents, multi-faceted records and record-filing project execution processes. As a domestic joint venture company seamlessly connected to local research base, we adapt to the complex and changeable clinical research environment in China by supporting genetic office declaration and sample entry.

In addition, in terms of data management, we provide database establishment and maintenance, data transfer, storage, and real-time online reporting to report safety results within 24 hours, assuring the safety and high-quality test data of clinical trials.

Teddylab always focuses on serving clinical research, pharmaceutical companies, researchers and customers in the diagnostic industry. We provide the highest quality regular internal training system, the latest policy interpretation and case sharing and GCP&GCLP training.

Data management system aiming at registration and application

Nearly 90% of the data in drug clinical trials comes directly from the central laboratory. The assurance of data quality not only affects the smooth progress of the entire clinical trial, but also directly affects the future NDA application. Teddylab always pays attention to the accuracy, scientificity and traceability of data in the process of clinical trials. With the support of a complete electronic system and a rigorous quality control system, Teddylab can provide real-time monitoring of sample data, timely and accurate online reports, and data transfer and comparison with hospitals or third-party data systems. Teddylab has an independent cloud backup system, which can support free online data storage services for up to 15 years to ensure that your project data meets the requirements of registration and application.