Analytical Assay & Potency
High-Performance Liquid Chromatography (HPLC) and spectroscopic assays to confirm precise active dosage strengths.
Quality Commitment
Quality at Every Step of the Lifecycle
We partner exclusively with qualified pharmaceutical manufacturing facilities to deliver safe, effective, and reliable formulations.
Quality Philosophy
Uncompromising standards across all formulations.
At Habbatus Pharmaceuticals, quality is not a final checkpoint—it is built into every phase of the product lifecycle.
We collaborate with modern manufacturing facilities equipped with automated tableting, liquid filling, blister packing, and fully equipped quality control laboratories. Every batch is supported by a comprehensive Certificate of Analysis (COA).
Regulatory Compliance
Our processes strictly follow the Drugs and Cosmetics Act and Rules governed by the Central Drugs Standard Control Organisation (CDSCO), India.
WHO-GMP Certified
WHO-GLP Certified- Schedule M compliance at all manufacturing partner sites
- Validated sanitization and cleanroom standards
- Documented retention samples and batch records
Process Workflow
The Six Stages of Quality Assurance
From pre-formulation screening to professional distribution, every milestone is systematically verified.
01
Formulation Development
Scientific formulation design targeting optimal therapeutic efficacy, stability, and patient palatability.
02
Raw Material Testing
Rigorous analytical verification of Active Pharmaceutical Ingredients (APIs) and pharmaceutical-grade excipients.
03
GMP Manufacturing
Production executed in certified facilities complying with Good Manufacturing Practices and validated cleanrooms.
04
Quality Control & Assay
Batch-wise assay testing, dissolution profiles, microbiological screening, and packaging integrity checks.
05
Secure Distribution
Temperature-monitored warehousing and tamper-evident transport to verified pharmaceutical stockists.
06
Post-Market Surveillance
Ongoing monitoring of product performance and structured regulatory feedback loops.
Analytical Testing
Rigorous Laboratory Protocols
Multi-stage testing guarantees chemical purity, dosage accuracy, and stability throughout shelf life.
Dissolution & Disintegration
In-vitro dissolution profiling ensuring prompt, consistent drug release for oral tablets and pediatric dispersibles.
Microbiological Screening
Stringent bioburden screening for oral liquids, mouthwashes, and topical dental gels.
Stability & Shelf-Life Verification
Accelerated and real-time stability testing under India-specific climatic zone conditions (Zone IVb).