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Metal Analysis Specialised Pharmaceutical Services

Eurofins | Chemical Analysis has vast experience in a large variety of sample analyses, ranging from routine pharmacopeial analysis to in depth problem solving. We offer a complete service of analytical testing, from method development to validation through to routine analysis. Whether a raw material, finished product or anything in between, Eurofins | Chemical Analysis has the solution to your analysis needs.

Routine Analysis
  • Pharmacopeial analysis (BP, Ph Eur, USP) via AAS or ICP-OES
  • USP <232> and  <233>
  • Extractable metals
  • Non-compendial analysis of raw materials and finished products
  • Product registration testing
  • Manufacturing process validation testing
Method Development
  • Extensive experience in large variety of sample matrices
  • Raw materials
  • Finished products (pharmaceutical drugs and complementary medicines, veterinary medicines)
  • Industrial samples
  • Highly sensitive (ppb detection)
  • Various digestion techniques via microwave, leaching or acid digestion
Method Validation
  • Method transfer
  • Method verification as per USP <1226>
  • Full method validation to ICH guidelines
Leachables and Extractables
  • In-process and stability samples
  • Low level analysis for arsenic contamination (VGA)
  • Investigations
  • Identification of unknown contamination in manufacturing processes
  • Batch to batch variations
All Items
  • Pharmacopeial analysis (BP, Ph Eur, USP) via AAS or ICP-OES
  • USP <232> and  <233>
  • Extractable metals
  • Non-compendial analysis of raw materials and finished products
  • Product registration testing
  • Manufacturing process validation testing
  • Extensive experience in large variety of sample matrices
  • Raw materials
  • Finished products (pharmaceutical drugs and complementary medicines, veterinary medicines)
  • Industrial samples
  • Highly sensitive (ppb detection)
  • Various digestion techniques via microwave, leaching or acid digestion
  • Method transfer
  • Method verification as per USP <1226>
  • Full method validation to ICH guidelines
  • In-process and stability samples
  • Low level analysis for arsenic contamination (VGA)
  • Investigations
  • Identification of unknown contamination in manufacturing processes
  • Batch to batch variations