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Latest from Sona Pharm:
Quality systems support and ongoing compliance through structured processes, documentation, and oversight — ensuring consistent product quality and audit readiness.
Pharmacovigilance support focused on patient safety and regulatory readiness — including safety case intake and processing, safety reporting, documentation management, and partner coordination.
End-to-end product registration and regulatory maintenance: strategy, dossier preparation, submissions, variations, renewals, labeling updates, and communication with health authorities.
Supply continuity through forecasting, planning, inventory control, distribution coordination, and risk management — keeping operations stable across markets.
Growth support through partner development, market assessment, launch planning, and portfolio expansion — tailored to complex, regulated environments.
Efficient market access through local-language packaging, regulatory-compliant pack adaptation, serialization and aggregation, with flexible reallocation across markets.
Partnerships with leading international manufacturers demonstrate our ability to meet rigorous standards and deliver consistently across projects.
Our team combines experience gained in international companies with deep knowledge of local regulated markets.
Unified processes and clear accountability ensure consistent quality and predictable performance across countries.
End-to-end product management combined with fast response, clear ownership and hands-on partner support.
