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Healthcare compliance
Healthcare Compliance
Ensure compliant relations and promotional materials
Veristat’s Legal support ranges from strategic advice with impact analyses of legislation on data protection and intellectual property to reviewing clients’ B2B contracts such as quality, pharmacovigilance and distribution agreements with external service providers.
Veristat's Compliance support includes advice on and review of interactions with healthcare professionals (HCPs) and healthcare organizations (HCOs), development and review of SOPs related to HCP/HCO-interactions, review of educational and promotional materials and presentations versus legislation and industry codes.
It's never too early to ensure healthcare compliance. Let's Talk.
Healthcare Compliance Across the Clinical Development and Commercialization Lifecycle
Contracting Support
- - B2B contracts
- - Quality agreements
- - PV agreements
- - Contract negotiation
Healthcare Compliance
- - Responsible person for Switzerland
- - Review of materials & HCP interactions
- - Advice on EU & Swiss industry codes
- - Compliance of product websites
Intellectual Property
- - Instruments
- - Copyrights
- - Policy developments
- - Advice on legal framework
Data Protection & Privacy
- - Gap Analysis
- - Impact Assessment
- - Advice on legal framework
Home >
why-veristat
company/about
approach
company/leadership-team
news
global-reach-locations
careers
careers/open-positions
veristat-culture-our-core-values
careers/explore-benefits
careers/life-at-veristat
because-we-care
why-veristat
therapeutic-expertise
therapeutic-expertise/oncology
therapeutic-expertise/neurology
endocrine-metabolic-disease
therapeutic-expertise/immunology-and-inflammation
therapeutic-expertise/infectious-disease
therapeutic-expertise/covid-19
therapeutic-expertise/cardiology
therapeutic-expertise/other
solutions
full-service-cro-biologics
cro-cell-gene
therapeutic-expertise/vaccines
therapeutic-expertise/rare-diseases
therapeutic-expertise/pediatric-clinical-trials
decentralizedclinicaltrials
clinical-trial-rescue-programs
services/full-service-solutions
clinical-trial-planning
clinical-trial-conduct
regulatory-submission
solutions/natural-history-studies
services
Services >
services/strategic-consulting
adaptive-designs
services/introduction-statistical-power
services/regulatory-affairs-overview
services/regulatory-affairs/regulatory-consulting-for-program-and-trial-design
services/regulatory-affairs/regulatory-approvals
services/chemistry-manufacturing-controls-cmc
services/regulatory-affairs/regulatory-agency-meeting-support
services/regulatory-affairs/regulatory-publishing
regulatory-medical-device-ivd
services/clinical-operations
services/clinical-operations/project-management
services/clinical-operations/monitoring
patient-recruitment-for-clinical-trials
patient-retention-and-site-engagement
medical-affairs-overview
services/medical-affairs/safety-pharmacovigilance
services/medical-affairs/data-monitoring-committees
services/medical-affairs/medical-monitoring-for-clinical-trials
services/regulatory-affairs/medical-writing
services/biometrics
services/biometrics/data-management
services/biometrics/biostatistics
services/medical-affairs/data-monitoring-committees
services/biometrics/statistical-programming
services/biometrics/standards-implementation
pharmacovigilance
services/strategic-resourcing
library
blog
latest-newsletter
contact-us
rfp
healthcare-compliance
Healthcare compliance