Full Support
We support our clients over the full medical product development lifecycle
Based in Central Europe
Palleos healthcare is a full-service research organization based in central Europe with a medical product focus.
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Founded in 2011
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Medical Product Focus
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Full-Service Portfolio
Product Development Lifecycle
Palleos' service segments focus on different areas of the product development lifecycle.
Consulting on Target Indication
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
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Consulting on Target Profile
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.
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Development Plan Consulting and Writing
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).
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Clinical Trial Services
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.
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Non-Interventional Trial Services
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.
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Clinical Trial Services
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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