World-Class Manufacturing & Quality Standards
Our Manufacturing Unit
At Maxtar Bio-Genics, manufacturing isn’t just a process—it’s a commitment to life. Our WHO-cGMP certified facility in Baddi, Himachal Pradesh, is built with advanced infrastructure designed for precision, scalability, and global compliance.
Our plant
integrates
Dedicated Beta-Lactam and General Manufacturing Blocks
State-of-the-art Equipment for blending, compression, coating, and encapsulation
Formulation Development Labs and walk-in stability chambers
Automated Packaging Lines that ensure hygiene and efficiency
Complete backward integration from raw material to finished product
We combine scientific rigor with operational efficiency, supported by a highly trained team of professionals committed to safety and quality
Manufacturing Capacity at a Glance
Tablets Production
Up to 5 million units per day
Capsules Production
Up to 0.5 million units per day
Quality That Inspires Confidence
Driven by stringent systems, validated processes, and regulatory compliance.
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At Maxtar Biogenics, quality is not just a function—it is embedded across every stage of our operations. From raw material procurement to final product dispatch, we follow a comprehensive quality management system aligned with WHO-GMP guidelines.
Consistent product quality across batches
Full traceability and documentation
Compliance with international regulatory standards
Reliable performance in diverse market conditions
Our approach ensures
Analytical Development & Microbiology Labs
Ensuring product safety, efficacy, and compliance at every stage.
Our state-of-the-art laboratories are equipped to perform advanced analytical and microbiological testing in accordance with pharmacopeial standards. These facilities support method development, validation, and routine quality testing.
Key capabilities include:
• Raw material and finished product testing
• Method development and validation
• Microbial limit and sterility testing
• Stability study support
Multilevel Quality Control
Integrated quality checks from input to output.
We implement a multi-tier quality control system that monitors every stage of the manufacturing process.
This includes:
Incoming raw material inspection •
In-process quality checks •
Batch-wise testing and validation •
Final product release by Quality Assurance •
This structured approach minimizes variability and ensures that every product meets defined specifications and regulatory requirements.
Regulatory Affairs Team
Supporting global market access with strong documentation expertise.
Our dedicated regulatory team works closely with international partners to facilitate product registrations across multiple markets. We provide end-to-end documentation support tailored to country-specific regulatory requirements.
Our expertise includes:
• CTD / ACTD dossier preparation
• Stability data generation
• Product registration support
• Compliance with semi-regulated and emerging market norms
Our quality system is designed not just to meet standards but to exceed them. Whether it’s for institutional tenders, branded generics, or private labels, we deliver with unwavering consistency.