IASON consulting assists pharmaceutical and biotechnology enterprises in defining milestones and critical path activities for your projects as well as in preclinical study management and monitoring.
Our experienced and multidisciplinary expert team critically reviews and assesses full preclinical development plans, non-clinical / clinical data, and documents on time.
Our independent IASON consulting experts in the fields of drug and medical device development confirm the accuracy and conformity with current standards such as legal requirements, GLP, ISO-norms, and SOPs. If applicable, we identify issues and provide constructive feedback for improvement before submission to legal agencies, such as Notified Bodies, EMA, or FDA.
IASON consulting treats every client and project with the uttermost confidentiality standards.
IASON consulting has the know-how and the experience to provide professional, critical, and confidential, review services for every scientific document within the pharmaceutical and biotechnological sector.
Find a short summary of the most common documents below, and please do not hesitate to contact us in case of any questions.
Follow the link below to find out more about the Scientific Document Support by IASON consulting
Feel free to contact us any time to receive more detailed information on your specific request.