Services
Operational clinical research services across Sweden, Norway and Denmark, delivered from a single point of contact.
— WHAT NORDIC TRIAL PARTNERS DELIVER
Three priority services across Scandinavia
Each service is delivered across Sweden, Norway and Denmark from a single point of contact, and across both pharmaceutical and medical device clinical research.
Study Start-Up
Site identification and feasibility, contract negotiations between sponsors, CROs and clinics, and regulatory and ethics committee submissions across Sweden, Norway and Denmark.
Site identification and feasibility assessments
Contract negotiations between sponsors, CROs and clinical sites
Ethics committee and competent authority submissions
CTIS submissions and EU Clinical Trials Regulation compliance
Site activation and readiness confirmation
Clinical Operations
Strategic and operational oversight of clinical programmes. Leading cross-functional teams in the planning and delivery of studies to scope, quality, budget and timelines. Including regulatory market authorisation submissions and lifecycle management. Programme and trial-level project management.
Programme and trial-level project management
CRO and vendor oversight
Cross-functional team coordination across Clinical, Regulatory, Data Management, Biometrics, Supply Chain and Labs
Regulatory compliance (EU, FDA, ICH)
Site Monitoring
Hands-on site monitoring across Sweden, Norway and Denmark, including inspection readiness, audit response and turnaround of underperforming sites.
Site monitoring visits and reporting
GCP audit and inspection readiness
Site relationship management with PIs and study staff
Investigator and study nurse support
— COVERAGE
Pharmaceuticals and medical devices
All services are delivered across both pharmaceutical and medical device clinical research, including work under the EU Medical Device Regulation (Regulation 2017/745) and ISO 14155:2026 on the device side.