Quality Systems & Standards
Quality systems designed for pharmaceutical consistency & trust.
At Nexovion Pharma, we are partnered with eminent manufacturers with their Research and Development centers to make our formulations with strong clinical insights such as raw material purity, API approved formulation, and DCGI approved therapies. All the above, we adhere with modern pharmaceutical technology and focus on high quality formulations.
We focus on patient-centric dosage forms, bioavailability, and regulatory readiness across five therapeutic categories.
HPLC Analytical Testing
Continuous batch quality verification
Compliance Architecture
Regulatory & Quality Assurance Foundations
WHO-GMP Aligned
Partner manufacturing facilities adhere to World Health Organization Good Manufacturing Practices.
DCGI Guidelines
Strict compliance with Central Drugs Standard Control Organisation regulatory directives.
ISO 9001:2015 QA
Standardized quality management systems governing handling and document management.
Temperature Sensitivity
Strict quality control handling for heat-sensitive liquid formulations and injectables.
Quality Protocol
4-Stage Batch Verification System
Every batch of medication distributed by Nexovion Pharma undergoes mandatory analytical verification.
Raw Material & API Assay
100% testing of Active Pharmaceutical Ingredients (APIs) and excipients against pharmacopeial standards before release into production.
Quality Checks:
In-Process Quality Checks (IPQC)
Continuous monitoring during granulation, compression, coating, and filling to ensure uniform content and hardness.
Quality Checks:
Finished Product Testing (FPQC)
High-performance liquid chromatography (HPLC) and dissolution profiling for every batch prior to release.
Quality Checks:
Product Traceability
Batch QR code tracking, retention sample archiving, and post-market safety monitoring.
Quality Checks:
Technical & Quality Desk
We maintain direct contact channels for healthcare providers and trade partners to reach our quality team.