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Marketaccess reimbursement
Market Access & Reimbursement
Securing early access and reimbursement for your products
Veristat Market Access team members provide strategic advice on national early access programs, write HTA/reimbursement dossiers for submission to national HTA bodies and prepare documentation for liaison with private healthcare insurance.
Furthermore, our team supports clients with joint EMA/HTA scientific advice meetings to optimize development plans for successful regulatory and reimbursement approvals.
It's never to early to start. Let's Talk.
Reimbursement Solutions Across the Clinical Development and Commercialization Lifecycle
Market Access Roadmap
- - P&R Strategy
- - Routes to Market Access
- - Early Access Reimbursement
- - Value-based contract solution

Health Technology Assessment (HTA)
- - Dossier strategy
- - Value dossier
- - National HTA dossiers
- - Price review

Pricing
- - Competitor Analysis
- - Pricing Analyses & Strategy
- - Negotiation
- - Price Optimization tactics

Payor Authority Management
- - Payor and HCP Research
- - Objection Handling
- - Advisory Boards
- - KOL liaison

Home >
why-veristat
company/about
approach
company/leadership-team
corporate-responsibility
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
marketaccess-reimbursement
Marketaccess reimbursement