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At Glasschroeder clinical science services, our aim is to strengthen and accelerate the process of translating laboratory discoveries into new treatments for patients.
The development of new drugs requires a lengthy process of clinical trials and regulatory procedures leading to market approval. Along with increasing complexities of conducting clinical research, the barriers between basic and clinical research are growing. This drives the demand for enhanced development strategies including innovative clinical trial designs and the corresponding standards-compliant documentation.
We support you in designing, developing, and implementing clinical research solutions to meet your specific needs. With more than 20 years of experience in clinical development and basic research, our goal is to help evaluate and optimize the potential of your drug candidate with a strong focus on early phases of clinical development and translational medicine.
We create documentation that regulatory agencies require during the clinical development from first in human to market approval of investigational medicinal products. We also generate documents for the medical and scientific society that describe results effectively and clearly. In summary, we provide well-structured documents that present information precisely and make sure the documents comply with regulatory, journal, or other guidelines.
We offer professional training on clinical research activities to develop your peoples' skills and knowledge. Courses can be designed for different levels to address the specific needs of your staff and according to the demands of complex global drug development programs.
|© Glasschroeder, 2014, all rights reserved Dr. rer. nat. Birgit Glasschröder|