Browse allPalleosCRO · GermanySite management, clinical development services and clinical monitoring.Request a quoteAsk about this companyWebsite (opens in a new tab)What they doTesting & analysisMedical device testingClinicalSite managementClinical development servicesClinical monitoringClinical data managementBiostatisticsPharmacovigilanceMedical monitoringMedical writingRegulatory & qualityRegulatory affairsFrom their websiteClinical study managementClinical study management (opens in a new tab)Project management (opens in a new tab)Stream CTMS (opens in a new tab)Medsci consulting and excellenceClinical study design (opens in a new tab)Regulatory supportClinical study approval (opens in a new tab)Feasibility servicesStudy feasibility (opens in a new tab)Country feasibility (opens in a new tab)Market access for medical devices in ceeDevice registration support (opens in a new tab)Dossier audit and amendment (opens in a new tab)New offering gcp trainingsGCP refresher course (opens in a new tab)BiometricsAdaptive designs (opens in a new tab)Bayesian inference (opens in a new tab)Decision theory (opens in a new tab)Machine learning (opens in a new tab)Statistical analysis plan (opens in a new tab)Veeva CDMS (opens in a new tab)Medidata Rave (opens in a new tab)SafetyMedDRA coding (opens in a new tab)Electronic safety reporting (opens in a new tab)ICSR processing (opens in a new tab)Show all (26)Clinical study management24/7 eTMF access (opens in a new tab)Regulatory supportFDA submissions (opens in a new tab)EMA submissions (opens in a new tab)Market access for medical devices in ceeTechnical testing (opens in a new tab)Toxicological testing (opens in a new tab)Clinical testing (opens in a new tab)Quality & certificationsGCP compliance (opens in a new tab)European Medical Writers Association (opens in a new tab)