Analytical Method Development
We provide the service of developing new analytical methods for testing Pharmaceutical drug substances across various dosage forms, excipients, and APIs.
"If you have an analytical problem, we have the solution."
Specialized Development
- • Assay of single/fixed dose combinations
- • Stability indicating assay methods
- • Related substances profiling methods
- • Stress studies & Stress degradation
Compliance & Validation
All methods are fully validated as per current ICH guidelines Q2(R1).
Developed hundreds of validated methods published in reputed journals.
Analytical Method Validation
Ensuring pharmaceutical procedures are suitable for intended analysis through a rigorous, systematic process.
STP Sharing
Analytical method shared as Standard Testing Procedure.
Draft Protocol
Method validation protocol developed after STP approval.
Client Review
Protocol submitted for client approval & recommendations.
Final Issuance
Finalized validation protocol is officially issued.
Study Initiation
Validation studies carried out strictly as per protocol.
Draft Report
Report prepared and submitted with raw data.
Final Report
Final copy with chromatographic soft data submitted.
Regulatory Help
Support for regulatory queries and extra experiments.
Stability Testing
Integral solution for shelf life estimation during product development, registration in global markets, and routine manufacturing monitoring.
Finished Product Testing
- Product release testing
- Form 39 Govt reports
- Process validation
- Market complaints
- Pre-shipment inspection
API Testing & Confidentiality
We perform Assay, Related Substances, and Stress studies on APIs. We ensure strict data security—your API methods are never disclosed to other customers.
Column Equivalency & Apps
Application support for existing methods. We adapt your methods to our brand columns to reduce time, effort, and organizational cost significantly.
Academic & Industrial Training Center
Bridging the gap between education and industrial excellence through expert-led scientific training.
Sophisticated Instruments
Practical and theoretical handling of HPLC, UPLC, IR, UV, NMR, and Mass Spectroscopy.
Dissertations & Projects
Support for M.Sc/M.Pharm/B.Pharm thesis from initiation to peer-reviewed journal publication.
Interview Preparation
Mock interviews (Technical/HR), Group Discussions, and direct job fixing through industry tie-ups.
Interpretation & Spectral Analysis
Mastering extraction, isolation, and characterization of drugs from Natural products.
Industrial Guidelines
Awareness of major organizational guidelines required for Production, QA, and R&D roles.
Abstract & Paper Writing
Expert guidance on writing research abstracts for international seminars and conferences.