Cutting-Edge Research in Vaccine & Drug Development
Kundli Specific
Drug Testing Services
Ensure your pharmaceutical products are safe, pure, and market-ready with our cutting-edge Drug Testing solutions. Our Kundli facility is US-FDA accredited, ensuring globally recognized standards and compliance.
Why Choose Our Drug Testing?
- Rapid, accurate results —ensuring your development stays on schedule
- Validated by US-FDA —rigorous quality controls at our Kundli lab
- Comprehensive testing profiles to meet global regulatory demands
- Expert technical team with extensive experience in pharmacopeial procedures
- Transparent reporting—clear, shareable, and audit-ready documentation
Our Key Offerings
- 1. Identification & Purity Analysis
Confirm your API identity and quantify purity levels in line with pharmacopeia guidelines.
- 2. Impurity & Degradation Product Screening
Detect known and unknown impurities; stability-indicating assessments ensure safety throughout shelf-life.
- 3. Assay & Potency Verification
Accurate measurement of active pharmaceutical ingredients to support formulation and dosage properties.
- 4. Residual Solvent & Toxicity Evaluation
Gas chromatography and toxicity testing to confirm safety in line with ICH guidelines.
- 5. Microbiological & Elemental Impurities Testing
Bacterial and fungal contamination analysis, heavy metals detection (ICP-MS/OES) for product compliance.
- 6. Stability Testing & Shelf-life Predictions
Accelerated and long-term studies using climate-controlled chambers, with comprehensive evaluation of degradation patterns.
Why Our Kundli Lab Stands Out
- US-FDA Accredited — Recognized rigor, reliability, and regulatory compliance
- State-of-the-art equipment — HPLC, GC-MS, LC-MS/MS, ICP-MS/OES, moisture analyzers, and stability chambers
- Skilled analysts — MSc-level experts proficient in method development and validation
- Global readiness — All reports and certificates meet ICH, WHO, and international client requirements
Streamlined Workflow
- 1. Consultation – Define your testing scope and schedule.
- 2. Sample Processing - Log, prep, and test at Kundli with secure tracking.
- 3. Analysis & Reporting – Receive detailed, easy-to-navigate digital and hard-copy reports.
- 4. Follow-up Support – Expert interpretation and result support for regulatory submissions or audits.
- Reach out
Let us help you speed up your drug development, ensuring quality and compliance every step of the way.
Contact our Kundli branch today to discuss tailored drug testing packages, timelines, or to request a formal quote..
INDIA
Drug Analysis & Pharmaceutical Testing Services
Drug testing is a critical process in the pharmaceutical industry, ensuring that medicines and active ingredients meet the required safety, quality, and efficacy standards. From raw materials to finished formulations, comprehensive analytical testing is essential to comply with regulatory guidelines set by authorities like the USFDA and WHO-GMP. We provide end-to-end drug testing solutions that support your product’s journey from development to market—reliable, regulatory-ready and USFDA-accredited.
Whether you’re in Bangalore, Delhi NCR, Gujarat, Mumbai, or anywhere in India, our advanced network ensures rapid turnarounds and high-quality results.
- Why Choose Our Drug Testing?
- USFDA‑Accredited & cGMP‑Compliant
Our labs meet USFDA standards under 21‑CFR, along with NABL/ISO 17025 accreditation—guaranteeing compliance at both national and global levels.
- Comprehensive Test Suite
We cover the full spectrum of drug testing, including:
- APIs, excipients, bulk drugs, finished and semi-finished products
- Pharmacopeial tests (IP, USP, BP, EP, JP) and custom client protocols
- Assay, impurities, related substances, residual solvents, heavy metals, extractables & leachables
- Physical characteristics: disintegration, dissolution, friability, water content, ash, particle size—tested with state-of-the-art HPLC, GC, LC-MS/MS, ICP-MS, UV, Karl Fischer, FTIR
- Microbiology: sterility, bioburden, endotoxin (LAL), antimicrobial efficacy, MIC, ZI—plus environmental monitoring
- Method Development & Validation
We design, validate (per ICH Q2, FDA guidelines), and transfer analytical methods across labs, supporting R&D through commercial scale, ensuring reproducible data and regulatory robustness.
- End‑to‑End Regulatory Support
From stability studies to Form‑39 release, packaging testing, container‑closure integrity, formulation development—all tailored for domestic approval and global export compliance.
- Multi-Location Presence, Single Standards
We operate from multiple sites—Bangalore, Delhi NCR, Gujarat, Mumbai, Kerala, and Andhra Pradesh—all aligned to the same SOPs, QA standards, and audit-ready documentation.
Key Advantages at a Glance
| Feature | Your Benefit |
|---|---|
| USFDA & NABL/ISO 17025 Accreditation | Trusted for both Indian and global pharmaceutical markets. |
| Advanced Instrumentation | Accurate trace-level detection using HPLC, LC-MS/MS, ICP-MS, GC-MS, Malvern, FTIR, UV |
| Pan-India Accessibility | Fast sample logistics and consistent service, no matter your region. |
| Regulatory-Grade Reports | Form-39, stability, export documentation—industry-ready |
| Flexible & Scalable Testing | Ideal for everything from clinical batches to full-scale production |
Our Lab Locations
Bangalore (Head Office)
Banaswadi, Kasturi Nagar
Delhi NCR
Kundli, Sonipat
Gujarat
Unjha & Ahmedabad
Kerala
Kochi
Andhra Pradesh
Guntur, Chittoor, Sri City
Rajasthan
Barmer
Maharashtra
Navi Mumbai
West Bengal
Kolkata
Serving India’s Pharmaceutical Industry
From raw materials to finished dosage forms, our drug testing services are trusted by manufacturers, formulators, CROs, and exporters. We help you meet FDA, CDSCO, EMA, MHRA, and other global regulatory standards for market entry and ongoing quality assurance.
Get Started with Eureka
Partner with a testing lab that brings USFDA accreditation, India-wide service and regulatory-grade confidence to your drug development and quality control.
Enquire today to discuss your specific drug testing needs—whether for routine QC, regulatory validation, stability studies, or export documentation. Let’s ensure your products meet the highest standards—globally.
