Certifications & Quality Standards

We operate under the most stringent regulatory frameworks to ensure every medication that leaves our plant meets peerless safety and efficacy benchmarks.

Globally Recognized Benchmarks

Our facility is regularly audited by international regulatory bodies to maintain our reputation as a leader in **pharmaceutical manufacturing excellence**.

WHO-GMP Certified

Rigorous adherence to World Health Organization Good Manufacturing Practices, ensuring safety and clinical consistency across all dosage forms.

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ISO 9001:2015

Committed to a robust Quality Management System (QMS) that streamlines every phase of product development and distribution.

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DCGI Approved

Full compliance with the Drug Controller General of India guidelines for clinical trials and pharmaceutical manufacturing approvals.

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GLP Standards

Good Laboratory Practices (GLP) followed in our advanced R&D centers to deliver scientific accuracy in testing.

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Total Quality Management (TQM) Framework

Our commitment to **High-Quality Pharmaceutical Manufacturing** is reinforced by our extensive TQM framework. We ensure that every tablet, injectable, and syrup undergoes multi-level screening before reaching the healthcare market.

  • Rigorous Raw Material Validation
  • In-Process Quality Checks (IPQC)
  • Stability Testing & Shelf-life Analysis
  • Post-Marketing Surveillance Compliance

Our Regulatory Pledge

At Novatrix Formulations LLP, certifications are not just milestones; they are our **Pledge to Patient Safety**. Every process meets the global benchmarks required for reliable healthcare therapy.

100%Compliance Rate
ZeroDefect Goal

The Quality Journey: Source to Success

Our multi-stage quality control protocol ensures that every formulation adheres to international clinical standards.

01

Raw Material Testing

Rigorous biological and chemical assay testing of all active ingredients before processing.

02

In-Process Control

Real-time monitoring of granulation, compression, and coating parameters.

03

Stability Studies

Accelerated and real-time stability testing to ensure shelf-life efficacy.

04

Final Validation

Comprehensive clinical validation and microbial testing before the final dispatch.

Advanced R&D & Testing Instrumentation

Our certifications are backed by a state-of-the-art laboratory environment, equipped with the latest **analytical instrumentation** to detect even the smallest discrepancies.

HPLC & Gas Chromatography
UV-Vis Spectrophotometry
FTIR Analysis
Dissolution Testing Apparatus
Microbiological Assays
Stability Chambers
Testing Lab

Alignment with Global Regulatory Bodies

Novatrix Formulations LLP proactively aligns its manufacturing protocols with several global regulatory guidelines, ensuring that our **Third-Party Pharma Manufacturing** and **PCD Franchise** partners can trade with absolute confidence in both domestic and international markets.

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