Analytical Services
Why Choose Our Analytical Services?
At Padm Lab, our analytical services are designed to give pharmaceutical companies complete confidence at every stage of drug development. From method development and validation to impurity profiling and advanced spectroscopy, our skilled analysts ensure accuracy, compliance, and reliability. With modern instruments and regulatory-approved facilities, we deliver results that meet global standards while keeping timelines intact.
Ensures accuracy and compliance for global regulatory submissions
Wide expertise covering APIs, drug products, and impurities
Reliable results backed by stringent documentation and QC checks
Faster turnaround without compromising quality
Our Capabilities
Method Development & Validation
Development of robust methods for APIs and finished drug products.
Validation as per ICH guidelines or customized client requirements.
Impurity Profiling & Characterization
Nitrosamine Screening & quantification by LC-MSMS
Residual Solvent Analysis by GC-HS
Advanced Spectroscopy & Analysis
Comprehensive structural analysis using FT-IR and NMR (1H, 13C- NMR, COSY, HMQC, etc.).
Thermal and physical property testing with DSC, TGA, viscosity, and elemental analysis.
Quality Control Testing
Routine QC studies including LOD, moisture content, residual solvents, and SOR.
Dissolution testing for finished drug products to ensure bioavailability standards.
Method Transfer & Scale Support
Smooth transfer of validated analytical methods between facilities.
Reliable support for long-term stability studies under cGMP conditions.
At Padm Lab, analytical testing isn’t just a service — it’s a commitment to safety, reliability, and trust. We provide the data and insights that pharma companies need to move forward with clarity and confidence.
Why Choose Our Analytical Services?
At Padm Lab, our analytical services are designed to give pharmaceutical companies complete confidence at every stage of drug development. From method development and validation to impurity profiling and advanced spectroscopy, our skilled analysts ensure accuracy, compliance, and reliability. With modern instruments and regulatory-approved facilities, we deliver results that meet global standards while keeping timelines intact.
Ensures accuracy and compliance for global regulatory submissions
Wide expertise covering APIs, drug products, and impurities
Reliable results backed by stringent documentation and QC checks
Faster turnaround without compromising quality
Our Capabilities
Method Development & Validation
Development of robust methods for APIs and finished drug products.
Validation as per ICH guidelines or customized client requirements.
Impurity Profiling & Characterization
Nitrosamine Screening & quantification by LC-MSMS
Residual Solvent Analysis by GC-HS
Advanced Spectroscopy & Analysis
Comprehensive structural analysis using FT-IR and NMR (1H, 13C- NMR, COSY, HMQC, etc.).
Thermal and physical property testing with DSC, TGA, viscosity, and elemental analysis.
Quality Control Testing
Routine QC studies including LOD, moisture content, residual solvents, and SOR.
Dissolution testing for finished drug products to ensure bioavailability standards.
Method Transfer & Scale Support
Smooth transfer of validated analytical methods between facilities.
Reliable support for long-term stability studies under cGMP conditions.
At Padm Lab, analytical testing isn’t just a service — it’s a commitment to safety, reliability, and trust. We provide the data and insights that pharma companies need to move forward with clarity and confidence.
Why Choose Our Analytical Services?
At Padm Lab, our analytical services are designed to give pharmaceutical companies complete confidence at every stage of drug development. From method development and validation to impurity profiling and advanced spectroscopy, our skilled analysts ensure accuracy, compliance, and reliability. With modern instruments and regulatory-approved facilities, we deliver results that meet global standards while keeping timelines intact.
Ensures accuracy and compliance for global regulatory submissions
Wide expertise covering APIs, drug products, and impurities
Reliable results backed by stringent documentation and QC checks
Faster turnaround without compromising quality
Our Capabilities
Method Development & Validation
Development of robust methods for APIs and finished drug products.
Validation as per ICH guidelines or customized client requirements.
Impurity Profiling & Characterization
Nitrosamine Screening & quantification by LC-MSMS
Residual Solvent Analysis by GC-HS
Advanced Spectroscopy & Analysis
Comprehensive structural analysis using FT-IR and NMR (1H, 13C- NMR, COSY, HMQC, etc.).
Thermal and physical property testing with DSC, TGA, viscosity, and elemental analysis.
Quality Control Testing
Routine QC studies including LOD, moisture content, residual solvents, and SOR.
Dissolution testing for finished drug products to ensure bioavailability standards.
Method Transfer & Scale Support
Smooth transfer of validated analytical methods between facilities.
Reliable support for long-term stability studies under cGMP conditions.
At Padm Lab, analytical testing isn’t just a service — it’s a commitment to safety, reliability, and trust. We provide the data and insights that pharma companies need to move forward with clarity and confidence.
Partner With Padm
Labs Today!
Connect with us today
Partner With Padm
Labs Today!
Connect with us today
Partner With Padm
Labs Today!