Commitment to High Quality and Excellence
Thanks to our multidisciplinary and knowledge-driven approach, we can deliver a broad variety of services across the full life cycle of your product.
To complement your drug development and shorten the time to market, Tigermed offers regulatory services for a wide range of products; from small molecules to biologicals and medical devices. Tigermed has successfully supported thousands of companies in both local trials and global projects and enabled them to provide solutions for unmet patient needs.
From start-up to close-out, our experienced clinical operation teams ensure efficient site support, patient safety and data monitoring through a complete project management system and effective relationships with widely distributed study sites. Our wide network of clinical experts ensures global consistency and high standards that meet ICH-GCP guidelines, wherever we manage your clinical trials.
With well-established Standard Operation Procedures and In-depth knowledge of industry standards and best practices, we are dedicated to providing high-quality, timely and cost-effective Data Management, Biostatistics and Statistical Programming services to support clinical development and regulatory submissions.
By combining our professional knowledge and Tigermed’s technical capabilities like testing, imaging analysis, drug safety, pre-clinical services, etc., we are able to offer complete solutions throughout the entire clinical trial. And, by integrating our full services chain in clinical research, we are able to help our clients save both time and costs.
As one of the largest MD and IVD regulatory and clinical trial CRO service provider in China, Tigermed and its over 300 full time experienced medical device clinical research professionals, have established long-term cooperative relationships with over 1700 manufacturers from more than 30 countries throughout the last 20 years.
The use of real-world data is growing rapidly in clinical development. With our in-house capabilities we can help you turn this real-world data into real-world clinical evidence. We offer one-stop high-quality services like retrospective/prospective RWS, post-marketing new drug safety monitoring, health economics study, real-world patient management to support drug/medical device full life cycle management.