Full Support
We support our clients over the full medical product development lifecycle
Palleos healthcare is a full-service research organization based in central Europe with a medical product focus.
Founded in 2011
Medical Product Focus
Full-Service Portfolio
We support our clients over the full medical product development lifecycle
Palleos' service segments focus on different areas of the product development lifecycle.
Palleos employs a stepwise process for the identification an prioritization in association with a compound whose indication has not yet been assigned by ist developer. The process balances ressources and comprehensiveness
read more...palleos healthcare assists in defining a Target Product Profile - a document installed to facilitate the process that navigates toward the approval of a medical product and a key tool to communicate with investors, authorities and other third parties.
read more...palleos healthcare consults and assissts in creating the development plan. It represents a detailed summary of the entire preclinical and clinical research strategy to define the critical path for the development program of an investigational product (i.e. drug or medicinal product).
read more...Palleos provides services for Phase I-IV clinical trials and medical device studies ranging from planning to closure of the study and offering profound expertise in Project Management, Regulatory Affairs, Monitoring, Data Management, Medical Writing & Medical Monitoring, Safety & Pharmacovigilance and Statistics, always keeping in mind the individual needs of every client.
read more...Non-interventional and observational trials become incerasingly important to suppyl information on drug use after its market approval during routine clinical application. Depending on your individual preferences and needs, palleos takes on the entire process of your study – from registration to final evaluation.
read more...Palleos is a full-service clinical research organization (CRO) providing services for Phase I-IV clinical trials ranging from planning to closure of the clinical study and offering profound expertise in Project Management, Regulatory Affairs, Monitoring, Data Management, Medical Writing & Medical Monitoring, Safety & Pharmacovigilance and Statistics, always keeping in mind the individual needs of every client.
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