Analytical Methods Development & Validation
THE ANSWERS YOU NEED, WHEN YOU NEED THEM.
Why choose Metrics for method development and validation? This simple analysis shows you the reasons.
THE METRICS DIFFERENCE
- A veteran staff
- State-of-the-art laboratories and equipment
- FDA and DEA registered and inspected
- Intuitive approaches to poorly soluble and complex compounds
- DEA II-V
- Potent and toxic capabilities
AND WHAT IT MEANS FOR YOU
- Your most aggressive timeline will be met.
- You’re assured of analytical methods that are practical and transferable
- Your point of contact is an industry veteran from whom you’ll receive one-on-one consultation.
- Complete, quality systems in place
- Competitive pricing
Wide range of compounds handled:
- Potent
- Toxic
- Light–sensitive
- Temperature–sensitive
- DEA II–V
- Other challenging molecules
Dosage forms:
- Tablets
- Capsules
- Suspensions
- Transdermals
Metrics provides various levels of method validaton — from abbreviated qualification to support early–phase studies to full ICH–compliant validation for late–phase and commercial products.
Method Development and/or Validation for:
- Chromatography (LC and GC)
- Dissolution (UV and LC finish)
- Moisture (Karl Fischer)
- Particle Size (Malvern)
- Ion Chromatography (Dionex)
- AA/ICP
- FTIR
- Titrations
- Particulate Matter (HIAC)
- Cleaning Methods (LC and TOC)
