Empowering Healthcare Through Innovation
Advance Clinical Research Empire offers expert consulting and services for drug and medical device development, enhancing quality and efficiency in clinical trials and regulatory submissions.
About us
At Advance Clinical Research Empire (ACRE), we are dedicated to transforming the clinical research industry through innovation, precision, and excellence. Founded by a renowned expert with over 30 years of experience, our organization is committed to delivering unparalleled full services in the development of drugs, medical devices, in vitro diagnostics (IVD) and others, including clinical study designs, clinical trial management, data management and data analysis, medical writing, regulatory submissions, and professional training.
The founder of ACRE holds a Ph.D. in Molecular Biology from Kyoto University of Japan and completed her postdoctoral research at the University of Washington. Throughout her career, she has worked with leading healthcare, biotech, and biopharmaceutical companies, including Johnson & Johnson, Abbott Laboratories, Siemens Healthineers, Astellas, and Boehringer Ingelheim Vetmedica (BIVI), from basic scientific discovery research and development, clinical sciences and clinical trial management, to regulatory submission. Her innovative ideas, precise designs, and seamless execution have made an indelible impact, significantly contributing to the success of these companies.
With a strong track record of successfully completing complex projects, she has become known for introducing cutting-edge technology and processes that improve efficiency and outcomes. Under her leadership, ACRE is focused on leveraging expertise to streamline clinical research processes and related activities, reduce costs, and accelerate the development of high-quality healthcare solutions.
Our mission is to not only provide exceptional services and consulting but also empower the next generation of professionals in the clinical research industry through our comprehensive training programs.
At Advance Clinical Research Empire (ACRE), we are dedicated to transforming the clinical research industry through innovation, precision, and excellence. Founded by a renowned expert with over 30 years of experience, our organization is committed to delivering unparalleled full services in the development of drugs, medical devices, in vitro diagnostics (IVD) and others, including clinical study designs, clinical trial management, data management and data analysis, medical writing, regulatory submissions, and professional training.
The founder of ACRE holds a Ph.D. in Molecular Biology from Kyoto University of Japan and completed her postdoctoral research at the University of Washington. Throughout her career, she has worked with leading healthcare, biotech, and biopharmaceutical companies, including Johnson & Johnson, Abbott Laboratories, Siemens Healthineers, Astellas, and Boehringer Ingelheim Vetmedica (BIVI), from basic scientific discovery research and development, clinical sciences and clinical trial management, to regulatory submission. Her innovative ideas, precise designs, and seamless execution have made an indelible impact, significantly contributing to the success of these companies.
With a strong track record of successfully completing complex projects, she has become known for introducing cutting-edge technology and processes that improve efficiency and outcomes. Under her leadership, ACRE is focused on leveraging expertise to streamline clinical research processes and related activities, reduce costs, and accelerate the development of high-quality healthcare solutions.
Our mission is to not only provide exceptional services and consulting but also empower the next generation of professionals in the clinical research industry through our comprehensive training programs.
Comprehensive Research Services
Expert consulting for drug and device development, enhancing quality and efficiency in clinical trials.
Study Design and Clinical Trial Management
Streamlined management for effective clinical trials and regulatory submissions, ensuring compliance and quality.
Professional writing support for clinical documents, enhancing clarity and regulatory compliance.
Innovative programs designed to elevate industry standards and improve workforce capabilities.
Preparation of document packages for regulatory agencies review approval based on specific product requirements