Pharegis organises regulatory work around six connected practice areas. The navigation is structured by the client’s regulatory task, while the technical articles retain their established search URLs and regulatory detail.
Core practice areas
Medicinal Products & Lifecycle covers EAEU medicinal product registration, API registration in Russia, dossier variations and post-approval lifecycle work.
GMP & Inspections covers EAEU GMP inspection readiness, documentation control and inspection support.
Medical Devices covers medical-device registration, classification, technical documentation and evidence requirements.
Clinical & Preclinical Studies brings together Phase I–III and nonclinical resources used in support of medicinal product registration.
Regulatory Consulting covers pathway assessment, gap analysis and registration strategy.
Regulatory Glossary provides a reference layer for terminology used in Russian and EAEU pharmaceutical regulation.