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Quality built into every dose.

At Sarvear Pharmaceuticals, quality is not merely a standard — it is the foundation of every product we manufacture. Every batch of tablets and dry-powder injectable undergoes comprehensive quality testing using validated analytical methods before release.

GMP
Schedule M certified
ISO
Quality management
WHO
Upgradation in progress
100%
Batches tested
Quality Systems

Every stage governed by validated SOPs.

Our quality systems are designed to earn and keep the trust of large pharma partners. From raw-material intake to finished-goods release — every decision is documented and traceable.

In-house QC Laboratory

Validated analytical methods for identity, potency, purity and dissolution testing.

Experienced QA Team

Qualified pharmacists and QA professionals with decades of collective experience.

Validated Processes

All manufacturing processes and analytical methods are validated per current GMP.

Batch Traceability

Complete raw-material to finished-goods traceability for every manufactured batch.

GMP Compliance

Schedule M-GMP certified facility with WHO-GMP upgradation currently in progress.

Documentation Excellence

Batch manufacturing records, deviations, CAPA and change-control per regulatory norms.

Continuous Monitoring

In-process controls, environmental monitoring and stability testing across formats.

Regulatory Compliance

Documentation supports domestic (CDSCO) and international export requirements.

GMP
Schedule M – GMP CertifiedCurrent Good Manufacturing Practice
ISO
ISO Certified FacilityQuality management systems
WHO
WHO-GMP UpgradationIn progress
QC
In-House QC LaboratoryValidated analytical methods
QC Laboratory

Validated methods — documented at every step.

Our in-house Quality Control lab uses validated analytical methods for identity, potency, purity and dissolution testing.

Lab scientist pouring and analysing solutionsQuality Testing
VEEGO Tablet Dissolution Test ApparatusQC Instruments
Lab technician with spectrophotometerSpectrophotometry
Our Commitment

We don't just manufacture medicines.
We manufacture confidence.

Every product reflects our commitment to patient safety, quality and consistency.

Frequently Asked

Questions from manufacturing and franchise partners.

Sarvear specialises in Beta-Lactam and Cephalosporin dry-powder injectables and tablets, alongside broader oral solids, capsules, dry syrups, oral solutions, eye/nasal drops and topical formulations. The full list is available on the Manufacturing Capabilities page.
Sarvear Pharmaceuticals U.A. is the parent manufacturing company operating the Selaqui plant. Sympar Lifesciences is Sarvear's PCD (Propaganda cum Distribution) division that offers monopoly-based franchise opportunities to distributors and stockists across India.
The facility is Schedule M-GMP certified and ISO certified. WHO-GMP upgradation is currently in progress. All manufacturing takes place under validated processes with an in-house QC laboratory and experienced QA team.
Fill the enquiry form on the Contact page with your drug licence and territory of interest, or write to us at symparlifesciences@gmail.com. Our team will confirm territory availability, share the product list with net rates, and finalise the partnership.
Yes. Sarvear currently supplies to Africa, CIS nations, Lithuania, Russia, Latin America and other export markets. We provide the manufacturing-side documentation required for registration, including CoA, master formula records and stability data.
MOQ varies by dosage form. Dry-powder injectables and tablets typically start at one commercial batch; smaller trial batches may be accommodated for validation runs. For F.O.R. destination supplies, minimum order value is ₹50,000. Please contact our team for a formulation-specific quote.