Cyanta is Your Method Development Partner

Cyanta Analytical Services can help develop and validate methods for your drug or medical device development programs.

Our method development capabilities include:

  • Drug substances and excipients
  • Oral dosages (tablets, capsules)
  • Topical dosages (creams, ointments, lotions)
  • Liquid dosages (solutions and suspensions for oral, ophthalmic, otic and parenteral delivery)
  • Transdermal patches
  • Non-traditional methods (tensile strength, bio-adhesives)
  • Elemental impurities (Microwave digestion ICP-MS)

After a successful method development, we can validate your analytical method per appropriate ICH guidelines. Cyanta's scientists frame their method validation activities with a practical approach coupled with outstanding quality and sound scientific expertise.

Method Development Case Study

A client came to Cyanta with 24 methods that required development using current technologies by GC/MS, LC/MS, replacing antiquated, inefficient analytical techniques due to an audit finding. The client had been working on the finding for 6 months and was in jeopardy of missing the deadline. We developed the methods in 15 months, 3 months before the client's deadline. The client is continuing, to this day, to use Cyanta as their preferred vendor.