Rocketpharm® is a Polish Contract Research Organization providing clinical research services for pharmaceutical, biotech and CRO companies in drug & device clinical trials, including feasibility, Regulatory & EC submission, study start-up, monitoring, close-out activities and CRA outsourcing.
What can we do for you?
Regulatory Services
CTA submissions, regulatory maintenance, obtaining import/export approvals and EU Legal Representative services.
Patient Recruitment
Patient referral from nearby sites and other patient requirement methods do accelerate your recruitment rate.
Monitoring Services
Investigators Selection, Site Evaluation, Pre-Study, Monitoring and Close-Out Visits. Project management.
Site Management
Site initiation and motivation, GCP and ISO 14155 trainings. Payments to the Institutions, Investigators and Site Teams.
Study Documentation
Preparation and translation of study documents including consent form, patient diary, protocol summary and other.
Personnel Outsourcing
CRA and CTA outsourcing for your trials.