Quality by design
Building quality into every stage of development, not testing it in afterwards.
Quality & Compliance GMP certified
Quality is at the heart of everything we do
At Harvin labs, quality is not just a department — it is a commitment woven into every process, every product and every partnership, from raw material to released batch.
- 100% Quality commitment
- 15+ Years of excellence
- 35+ Products
- Pan-India Supply
Our quality framework
A system built to deliver consistently
A robust quality management system that keeps every batch of every product on specification.
Risk management
Proactive risk assessment and mitigation across every process and supplier.
Process control
Stringent in-process controls that keep every batch consistent and reliable.
Continuous monitoring
Ongoing monitoring and improvement, driven by data from every campaign.
People & culture
Trained, empowered teams who own the quality of what they make.
Compliance
Full compliance with applicable regulatory requirements and documentation.
Certifications
Audited, certified & documented
We adhere to the highest quality standards and regulatory guidelines — and every consignment ships with a batch-specific Certificate of Analysis.
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Valid until 02 Sep 2029
GMP Certificate of Compliance
Good Manufacturing Practice (GMP)
Scope of certification
Manufacturing and processing of Active Pharmaceutical Ingredient (API), intermediates and specialty chemicals including chemical synthesis, purification, drying and packing.
Certification cycle
- 03 Sep 2026 Initial registration
- 03 Sep 2026 Issued
- 02 Sep 2027 First surveillance
- 02 Sep 2028 Second surveillance
- 02 Sep 2029 Expires
From raw material to release
Quality at every step
From raw material selection to final delivery, every stage of the value chain has its own checks.
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01
Raw material
SelectionQualified grades, tested on receipt.
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02
Supplier
QualificationApproved vendors, audited and reviewed.
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03
In-process
ControlCritical parameters checked every batch.
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04
Quality
TestingHPLC, GC, IR and KF against specification.
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05
Pack &
ReleaseReleased only with a signed COA.
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06
Distribution &
SupportDocumentation and technical follow-up.
Reaction & synthesis suites
Advanced chemical manufacturing
GMP certified
facility
facility
Infrastructure & quality control
Driven by science. Committed to quality.
Our reaction facilities, analytical instrumentation and chemical engineers make sure every pharmaceutical intermediate we synthesise meets its quality benchmarks before it leaves the plant.
- Reaction systems Glass-lined and stainless steel trains
- In-process testing HPLC and GC during the batch
- In-house QC lab Release testing on site
- Full traceability Batch records retained
Partner with a quality-focused manufacturer
Let's build a healthier future together — with trust, transparency and quality you can document.