Our Services
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We provide full regulatory support for pharmaceutical and biotech manufacturers entering the Azerbaijani market.
Our services include:National registration and Recognition procedure
Dossier preparation and submission
Variations, renewals and labeling updates
Regulatory communication with the Ministry of Health
Compliance with local regulatory and safety requirements
Orphan drug listing
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We navigate the complex pricing and reference-pricing system in Azerbaijan to ensure sustainable and compliant market entry.
Our expertise covers:Pricing strategy & reference price analysis
Preparation of pricing submissions
Stakeholder engagement with key market access institutions
Hospital and national purchasing pathways
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We help manufacturers establish a strong and compliant commercial presence in Azerbaijan.
Our support includes:Launch planning & execution
Brand strategy and positioning
Hospital access and tender presence
KOL network development
Sales and demand generation activities
Post-launch monitoring and reporting
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We support partners in navigating Azerbaijan’s public procurement systems.
Services include:Tender monitoring and eligibility evaluation
Coordination with national distributors and procurement bodies
Hospital supply process support
Hospital consumption support
Pricing scenarios for public tenders
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We ensure compliant local safety procedures for manufacturers operating in Azerbaijan.
Local QPPV partnership
Case intake and reporting
Periodic safety updatesacovigilance (PV) & Safety Support
Safety documentation management
Compliance with national PV regulations
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NEXA Pharm acts as a trusted local partner for global pharmaceutical companies.
We offer:Representation of manufacturers in Azerbaijan
Flexible market entry models
Identification of commercial opportunities
Partnership negotiations
Ongoing strategic support for regional growth
At NEXA Pharm, we support global pharmaceutical and biotech manufacturers in entering, launching, and growing their presence in Azerbaijan. Our integrated services cover the full product lifecycle — from regulatory approvals to commercial execution — ensuring efficient, compliant, and successful market entry.

