Verification evidence is still being completed.
Inpharmatis
Riga, Latvia
- Verified lead
- Polina Dombure
- Lead status
- STATUS: VERIFIED APRIL 2026
- Leadership verification
- Founder and Chief Executive Officer
- 2026 technical specialization
- Regulatory Affairs, Pharmacovigilance, GMP and GDP Compliance, and eCTD Publishing
- Review cycle
- 24 April 2026
- Full address
- Raina bulvaris 11, 3rd floor, Riga, LV-1050, Latvia
- Site coordinates
- Verification evidence is still being completed.
- Editorial review
- Memel Biotech editorial review
- Official leadership source
- Pharma Tech Outlook feature naming Polina Dombure as CEO of Inpharmatis Group.
- Editorial note
- Riga regulatory consultancy with a named founder-CEO, multi-country pharmacovigilance and GMP auditing coverage across EU plus CIS, and a proprietary Prudenta eSolutions stack.
Regulatory Affairs, Pharmacovigilance, GMP and GDP Compliance, and eCTD Publishing
Pharma Tech Outlook recognition as Top Compliance Service Company Europe 2021, Public leadership disclosure on LinkedIn, Documented multi-country regulatory service scope
Riga regulatory consultancy with a named founder-CEO, multi-country pharmacovigilance and GMP auditing coverage across EU plus CIS, and a proprietary Prudenta eSolutions stack.
Riga regulatory consultancy with a named founder-CEO, multi-country pharmacovigilance and GMP auditing coverage across EU plus CIS, and a proprietary Prudenta eSolutions stack.
- Website
- inpharmatis.com
- Lead
- Polina Dombure (verified ↗)
- Compliance
- Not yet on record
- Last reviewed
- 24 Apr 2026 (1mo ago)
- Scale
- Regulatory consulting service delivery across EU and CIS
- Capabilities
- Regulatory Affairs in EU and CIS · Pharmacovigilance System Operation and QPPV · GMP and GDP Compliance Auditing
- Founded
- 2009
- Headcount
- 11-50
Polina Dombure
Founder and Chief Executive Officer
Inpharmatis contacts page listing Raina bulvaris 11 in Riga as the head office address.
Open sourceRegulatory consulting service delivery across EU and CIS
Riga, Latvia. Regulatory Affairs, Pharmacovigilance, GMP and GDP Compliance, and eCTD Publishing. Review completed on 24 Apr 2026.
Multi-jurisdictional regulatory advisory across EU and CIS
Pharma Tech Outlook recognition as Top Compliance Service Company Europe 2021, Public leadership disclosure on LinkedIn, Documented multi-country regulatory service scope
Regulatory Affairs, Pharmacovigilance, GMP and GDP Compliance, and eCTD Publishing
Riga regulatory consultancy with a named founder-CEO, multi-country pharmacovigilance and GMP auditing coverage across EU plus CIS, and a proprietary Prudenta eSolutions stack.
Inpharmatis offers a rare full-scope pharmacovigilance and regulatory consulting surface that bridges EU quality standards and CIS market access, anchored by a named founder-CEO and a proprietary eCTD and literature-monitoring toolset.
Core capabilities
Primary declared technical activities and areas of operating focus.
Verification source dossier
Official source set used to support leadership, physical-site, certification, and watch-note evidence.
Declared infrastructure
Quality system coverage
GMP / GLP / ISO-13485 / FDA-Inspected are global quality-system standards. "Verified active" means the directory confirmed the certification is current; "Review in progress" means the cert status is currently being re-verified.
- GMP
- REVIEW IN PROGRESS 2026
- GLP
- REVIEW IN PROGRESS 2026
- ISO-13485
- REVIEW IN PROGRESS 2026
- FDA-Inspected
- REVIEW IN PROGRESS 2026
Verification history
Frequently asked questions
- Where is Inpharmatis located?
- Inpharmatis operates from Raina bulvaris 11, 3rd floor, Riga, LV-1050, Latvia, Riga, Latvia.
- Who runs Inpharmatis?
- Inpharmatis is led by Polina Dombure, Founder and Chief Executive Officer. Verified 24 Apr 2026.
- What does Inpharmatis do?
- Riga regulatory consultancy with a named founder-CEO, multi-country pharmacovigilance and GMP auditing coverage across EU plus CIS, and a proprietary Prudenta eSolutions stack. Core capabilities: Regulatory Affairs in EU and CIS, Pharmacovigilance System Operation and QPPV, GMP and GDP Compliance Auditing.
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