Our Products

We are committed to manufacturing in compliance with international regulatory standards. Our facilities and processes are designed to meet the requirements of various global health authorities.
Quality Assurance & Quality Control
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WHO-GMP (Good Manufacturing Practices)
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ISO 9001:2015 (Quality Management Systems)
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Our facilities are designed to be audit-ready for USFDA, EMA, and other regulatory bodies.
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Environment, Health, and Safety (EHS) compliance.
Our Certifications & Commitments
We are committed to manufacturing in compliance with international regulatory standards. Our facilities and processes are designed to meet the requirements of various global health authorities.
Regulatory Compliance
Products Designed For You
Bulk Drugs (APIs) & Intermediates
We produce a wide spectrum of Active Pharmaceutical Ingredients (APIs) and critical intermediates that form the core of effective medicines. Our products are characterized by high purity, excellent bioavailability, and strict adherence to pharmacopoeial standards.
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Therapeutic Areas: [e.g., Cardiovascular, Antibiotics, Central Nervous System, Gastrointestinal, Antifungal, etc.].
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Custom Synthesis: We also offer custom synthesis and manufacturing services tailored to specific client requirements.

Finished Formulations
Our formulation units transform APIs into patient-ready medicines. We manufacture a variety of dosage forms in different strengths and pack sizes.
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Solid Dosages: Tablets, Hard Gelatin Capsules.
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Liquid Dosages: Syrups, Suspensions.
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Other Dosages: Ointments, Creams. (Mention Injectables if applicable)

Our Uncompromising Quality Standards
Quality is not just a department at VVSRA Healthcare; it is a mindset that permeates our entire organization.
Quality Assurance & Quality Control
Our rigorous QA/QC systems ensure every product batch meets its predefined specifications and regulatory requirements.
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State-of-the-Art Laboratories: Equipped with advanced analytical instruments like HPLC, GC, Spectrophotometers, etc.
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Stringent Testing: Raw materials, in-process samples, and finished products undergo exhaustive testing.
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Documentation: Meticulous documentation and batch record tracking ensure full traceability.
