Vitaccess Registries
Access the data through subscription, or partner with us on a bespoke registry study tailored to your evidence generation needs.
Our innovative multi-client syndicated registries support case-by-case RWE generation needs while improving study flexibility and speed for all stakeholders through harmonized governance, design, and data collection.
Access Vitaccess registry data to explore insights, accelerate research, and generate meaningful RWE
Act as a pre-launch registry Founder and influence decision-making on registry design and development
Subscribe to access an existing dataset and discover how Vitaccess can support your research goals
MyRealWorld MG
Vitaccess is providing the opportunity for novel research initiatives using the anonymized study dataset, including extended commercial subscriptions.
For more information on the MyRealWorld MG study or research opportunities using the study dataset, please contact us
Innovative multi-client syndicated registries
Flexibility
Cost
Stakeholders
Data
Recruitment
Flexibility
Our registries are designed to adapt to your research needs, providing unrivalled flexibility:
- Custom research options that align with your evidence plans
- Access to a “consent-to-contact” registry cohort to accelerate patient recruitment into clinical trials and other studies
- Tailored safety reporting for marketed products
- Opportunities to expand registries geographically or to new populations, such as pediatric patients
Cost
Vitaccess registries deliver value, combining high-quality data with efficient funding models:
- Subscribers benefit from shared funding, offering cost savings compared to independent registries competing for resources
- A registry with an engaged patient cohort sets the foundation for efficient accomplishment of multiple research projects
Stakeholders
Our registries bring together patients, clinicians, and pharmaceutical companies, supporting all key stakeholders:
- Comprehensive RWE solutions for Medical Affairs, Health Economics, Market Access, Safety, and Commercial teams
- Collaborative approach preferred by patient advocacy groups and key opinion leaders
- Synergies between Vitaccess and patient or clinician networks leverage deep experience to unite research, patient, and healthcare communities
Data
Vitaccess registries generate rich, actionable insights through integrated, patient-centered data:
- Combine patient- and clinician-reported information with medical record data
- Longitudinal data collection supports learning, evidence sharing, and faster research and therapy development
- Interactive online dashboards enable near real-time visualization of aggregated anonymous data for subscribers
Recruitment
Our registries accelerate recruitment through extensive networks and flexible approaches:
- Having a network of clinical centers to serve as study sites for a single registry is efficient for researchers, sites, and patients
- Options for hybrid recruitment using a combination of clinical sites, community physicians, patient advocacy groups, and digital campaigns
- Recruiting patients pre-product approval offers subscribers access to data from an engaged cohort at the point of product launch and potential treatment initiation
Patient‑first. Data‑driven.
Globally connected. 6
- Freight consolidation to reduce emissions and transportation costs.
- Use of electric trucks for short-haul and inter-facility transfers.
- Smart inventory transfers based on energy-efficient schedules.
- Waste-reducing return logistics for defective or excess products.
