Method Development/Method Validation

• Expertise and Experience
  – 4 Ph.D. Chemists and Highly Capable Bioanalytical Staff
• Reliability
  – Linearity Correlation Coefficient >0.99
• LOQs to 5 Picograms/mL
• Rapid Turnaround
  ­ 1-3 Days for Method Evaluation
• Typical Sample Run-time
  ­ 4-10 Minutes
• Recently Validated Methods for:
  17α-Ethynylestradiol
  5-fluorouracil (5-FU)
  Amikacin
  Avermectin / ivermectin
  Cefquinome sulfate
  Dextromethorphan and 3 metabolites
  Doxycycline
  Farnesylthiosalicylic acid (FTS)
  Fentanyl
  Flunixin
  GHRP-1
  Ketamine
  Leuprolide
  Lisinopril
  Lovastatin
  Mupirocin
  Omeprazole
  Oxybutynin
  Phosphorothiate oligodeoxynucleotides
  Sorivudine
  Sulfadiazine
  Thromboxane B₂ (TXB2)
  Thymosin α1
  Tilmicosin
  Trapidil
  Trimethoprim
  Zilpaterol