Intertek Pharmaceutical Services

Whitehouse, New Jersey, US

Intertek pharmaceutical services include contract laboratory services, regulatory guidance and supply chain assurance to support your unique pharmaceutical or biopharmaceutical outsourcing requirements.

Our pharmaceutical scientists and regulatory experts work with you at every stage of development, providing consistently high quality and flexible services that enable you to achieve a marketplace advantage. Over the last 20 years, our network of Good Laboratory Practice (GLP) or Good Manufacturing Practice (cGMP) laboratories and regulatory experts have provided high quality technical services which ensure Total Quality Assurance for some of the world’s largest and most innovative pharmaceutical companies.

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SPE

Solid Phase Extraction

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SPE (Solid-phase extraction)
SPME (Solid Phase Micro Extraction)

Headspace Gas Chromatography

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Residual Solvent Analysis

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Residual Solvents

USP <467>

Compendial Testing

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USP, EP, JP Compendial Testing

Quality Assurance

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Lot Release Testing

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GMP Batch Release Testing

Loss on Drying Testing

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FT-IR

Fourier transform infrared spectroscopy

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pH Measurement

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Karl Fischer Titration

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Coulometric or Volumetric

Melting Point Determination

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ICP-AES/OES

Inductively Coupled Plasma Atomic Emission Spectroscopy/Optical Emission Spectroscopy

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Polymer Characterization

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Polymer Formulation Compound Identification

ICP-MS

Inductively Coupled Plasma Mass Spectrometry

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HPLC-MS

High Performance Liquid Chromatography Coupled Mass Spectrometry

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Mass Spectrometry

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UV-VIS Spectroscopy

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Product Stability Testing

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cGMP Stability Studies

Raw Material Testing

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Packaging Consulting

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USP <1663> & USP <1664> Testing

Residual Impurity Analysis

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Micro FT-IR Analysis

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Material Testing Services

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HPLC

High Performance Liquid Chromatography

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Elemental Analysis

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C,H,N Analysis

Sulfur, Chlorine, Bromine, Iodine, Fluorine Analysis

Forced Degradation Studies

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Photostability Studies

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Extractable and Leachable Testing

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Extractable/Leachable services on drug product packaging and drug product

Solubility and Dissolution Testing

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Package and Container Testing

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Ion Exchange Chromatography

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Gas Chromatography (GC)

Gas Chromatography

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Certified Standards

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Analytical Validation

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Analytical Method Development

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Method Transfer and Method Verification

LC-MS

Liquid Chromatography-Coupled Mass Spectrometry

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Analytical Chemistry Services

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Optical Rotation

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High Resolution Mass Spectrometry

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GC-MS

Gas Chromatography Coupled Mass Spectrometry

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Chemical Stability Testing

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Experimental Design

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cGMP Method Development and Validation

Accelerated Stability Testing

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Accelerated & Real Time Stability Testing

Structure Determination

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AAS

Atomic Absorption Spectroscopy

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Graphite Furnace / Flame AA

LC-MS/MS

Liquid chromatography tandem mass spectrometry

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Unknown Material Identification

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Solventless Extraction

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HRAM LC-MS/MS

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High Resolution Accurate Mass (HRAM) LC-MS/MS

HRAM GC-MS

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High Resolution Accurate Mass (HRAM) Gas Chromatography-Mass Spectrometry

Atomic Emission Spectroscopy

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Specialty Mass Spectrometry Methods

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Imaging & Spectroscopy

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Spectrophotometry

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Product Quality Control

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Other Mass Spectrometry Methods

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Chromatography

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Spectroscopy

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Liquid Chromatography

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Chemistry and Materials

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Infrared Spectroscopy Services

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Liquid Chromatography Coupled Mass Spectrometry Methods

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ICH Stability Testing

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HPLC-MS/MS

High Performance Liquid Chromatography Coupled Tandem Mass Spectrometry

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Impurity Analysis

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Elemental impurities

CHQ3D Elemental Impurities

USP 232/233 Testing

Metals Testing

2018-05-21 16:52:44 UTC

Net Promoter Score of 10 received for Package and Container Testing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 8.

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