Method Verification – Confirming
Accuracy & Reliability for Your
Analytical Testing
Method verification is essential when a compendial method (e.g., USP, EP, BP, IP) is adopted in a laboratory for the first time, ensuring it performs as intended under actual testing conditions. Unlike full method validation, verification focuses on confirming accuracy, precision, and suitability of the method within the specific lab environment, instruments, and analyst expertise. At SIMA LABS, we conduct rigorous method verification in compliance with USP <1226>, Ph. Eur. 2.1.1, and other global pharmacopeial guidelines, ensuring your analytical results remain accurate, reproducible, and regulatorily accepted. Our process ensures seamless integration of established methods into your quality control workflows.
Why Choose SIMA LABS for Method Verification Testing?
- USP, EP, BP, IP-Compliant – Verification as per international pharmacopeial standards.
- Expert Analysts – Skilled in adapting compendial methods to specific lab and product needs.
- Advanced Instrumentation – HPLC, GC, FTIR, UV-Vis, ICP-MS, and more.
- Comprehensive Checks – Accuracy, precision, system suitability, and detection limits.
- Applicable Across Products – APIs, excipients, finished products, and stability samples.
- Regulatory-Ready Reports – Accepted for audits, submissions, and market approvals.
35+ Years of SIMA LABS – Method Verification Testing You Can Trust
SIMA LABS is NABL accredited and approved under FSSR and BIS for conducting method verification in accordance with USP <1226>, Ph. Eur., BP, and IP guidelines. Our verified procedures ensure that pharmacopeial methods adopted in our laboratory deliver consistent, accurate, and reproducible results, meeting both domestic and international regulatory requirements.
We provide method verification services to confirm that compendial methods are suitable for use in your specific testing environment.
Scope of Verification:
Applicable To: APIs, excipients, finished dosage forms, stability samples, and intermediates.
Verification Parameters:
Accuracy and recovery studies
Precision (repeatability & intermediate precision)
System suitability testing
Detection and quantitation limits (LOD/LOQ)
Specificity for intended analytes
Techniques Covered:
HPLC, GC, UV-Vis, FTIR, ICP-MS, ICP-OES
Microbiological and dissolution methods
Regulatory Compliance:
USP <1226>
European Pharmacopoeia (Ph. Eur.)
British Pharmacopoeia (BP)
Indian Pharmacopoeia (IP)
With experienced analysts, cutting-edge instrumentation, and globally recognized protocols, SIMA LABS ensures that every verified method is robust, reliable, and audit-ready.
Trusted by leading brands
our customers are the driving force behind our growth and innovation
Precision. Compliance. Innovation
Our Expertise
At Sima Labs, we specialize in advanced analytical testing, regulatory compliance, and quality assurance across the food, pharmaceutical, and environmental sectors—delivering reliable results with international standards and technical excellence.
Residue Analysis
SIMA LABS offers residue testing and compliance with ELV, RoHS, REACH, and EN71 standards
Microbiological Analysis
SIMA LABS provides microbiological testing and indoor air quality monitoring.
Molecular Biological Analysis
SIMA LABS offers GMO, allergen, pathogen testing, event identification, and pharma analysis for safety and compliance.
Method Development and Validation Studies
SIMA LABS provides stability testing, drug analysis, quality checks, lab consultancy, training, and R&D support.
Environment Monitoring
SIMA LABS offers environmental testing for pollutants, gases, and air quality monitoring.
Get In Touch
At SIMA LABS, we’re proud to offer our expertise in analysis and research to help you find the right solutions.
Let’s Connect – Book Your Appointment Today!
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+(91)-(11)-43854300