Quality Assurance for Pharma Excellence
Pharmaceutical products and their intermediates must meet the highest quality and safety standards. Our Drugs & Intermediates Testing Services ensure your formulations, APIs (Active Pharmaceutical Ingredients), and raw materials comply with national and international regulatory standards.
Why is Drugs & Intermediates Testing Important?
In the pharmaceutical industry, even the slightest impurity can impact product safety, efficacy, and compliance. Testing is essential to:
- Ensure batch-to-batch consistency
- Verify identity, strength, purity, and stability
- Detect contamination or degradation
- Meet regulatory guidelines from FDA, ICH, USP, EP, IP, and WHO
What We Offer
We provide comprehensive analytical testing for:
- Active Pharmaceutical Ingredients (APIs)
- Bulk Drug Intermediates
- Finished Dosage Forms (tablets, capsules, syrups, etc.)
- Excipients and Additives
- Raw Materials & Packaging Components
Our testing covers:
- Physico-chemical properties
- Assay (potency)
- Identification & Purity tests
- Related substance / impurity profiling
- Microbiological analysis
- Residual solvents, heavy metals, pH, moisture, and more
The Process
- Sample Submission – Collected or received as per pharmaceutical sampling protocols
- Advanced Lab Analysis – Using HPLC, GC, UV-Vis, FTIR, AAS, and other instruments
- Result Reporting – Detailed COA (Certificate of Analysis) with method references
- Compliance Support – Assistance with documentation for audits, submissions, and regulatory inspections
Industries We Serve
- Pharmaceutical Manufacturers
- Chemical & Intermediate Producers
- Exporters & Importers
- R&D Laboratories
- Third-Party Manufacturers and Formulators
Why Choose Us?
- GLP and NABL-accredited partner labs
- Compliance with pharmacopeial and regulatory standards
- Timely turnaround and expert consultation
- Strict confidentiality and data integrity
Assure Quality. Build Trust.
Contact us for high-precision testing of drugs and pharmaceutical intermediates.
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