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- darltesting@gmail.com
- +91 97173 24010
Pharma testing
Pharma Testing Services
Pharmaceutical testing services that ensure your products meet the highest standards of safety, efficacy, and regulatory compliance. Our ISO/IEC 17025 and NABL-accredited lab provides end-to-end testing for raw materials, APIs, excipients, finished products, and packaging materials in line with global pharmacopoeial standards.
Why Pharmaceutical Testing Matters
✅ Ensure product safety and therapeutic efficacy
✅ Prevent batch failures and costly recalls
✅ Meet national and international regulatory guidelines (IP, USP, BP, EP, ICH)
✅ Verify raw material quality and API strength
✅ Support stability studies and shelf-life claims
✅ Prevent batch failures and costly recalls
✅ Meet national and international regulatory guidelines (IP, USP, BP, EP, ICH)
✅ Verify raw material quality and API strength
✅ Support stability studies and shelf-life claims
Explore More Services
Pharmaceutical testing is crucial for ensuring the quality, safety, and efficacy of drugs and other pharmaceutical products. It encompasses a wide range of evaluations and assessments to verify that products meet regulatory standards, are effective for their intended use, and do not pose a risk to patients.

Raw Material & API Testing

Finished Dosage Form Testing

Packaging & Container Testing
Pharma Testing
Frequently Asked Questions
1. What types of pharmaceutical products do you test?
We test a wide range, including:
Tablets, capsules, injections, syrups
Ointments, gels, creams
APIs, excipients, herbal formulations
Packaging materials and containers
2. Do you follow pharmacopoeial standards like IP, USP, BP?
Yes, we test as per IP, USP, BP, EP, and ICH guidelines, ensuring compliance with national and global regulatory norms.
3. Do you offer stability studies and shelf-life testing?
Absolutely. We conduct both real-time and accelerated stability studies under ICH conditions, along with photostability, moisture, and thermal degradation testing.
4. Are your reports accepted by CDSCO and FDA authorities?
Yes. Our lab is NABL and ISO/IEC 17025 accredited, and our reports are accepted by CDSCO, State FDAs, and for international regulatory submissions.
5. Do you test APIs and raw materials?
Yes. We test APIs and excipients for identity, purity, potency, residual solvents, and other pharmacopoeial requirements.