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Registration strategy and Сonsulting
Budgeting
Registration strategy development
Study feasibility
Vendor selection
Data search and analysis
Clinical trials
Outsourcing CRAs in Russia and the EAEU
Development of medical documentation and biostatistics
Monitoring
Data-management
Patient home visits
Bioequivalence study
Therapeutic equivalence studies
Clinical trials of medical devices
Registration
Audit of the registration dossier
Bringing the registration dossier in compliance with the requirements of the EAEU
Conversion of registration dossier into XML format
PIL readability user testing
Translation of the Registration dossier
Turnkey registration
Post-authorization clinical studies
Phase IV studies
Non-interventional studies
Investigator-initiated studies
Post-authorisation safety study
Marketing research
Pharmacovigilance
QPPV in the EAEU
Safety monitoring of medical devices
Building a pharmacovigilance system
Safety in clinical trials
Pharmacovigilance audit
Pharmacovigilance contact person
Therapeutic expertise
Clinical trials in Oncology in the EAEU
Contact
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