Microbiology Testing Services

The diverse scientific capabilities within Toxikon's Microbiology Department are leveraged appropriately to address each unique product requirement. With the emergence of complex devices, such as combination products, our team has become recognized by the industry as a valuable resource in developing early stage screening studies to final product verification and validation studies. Our experience and direct interaction with regulatory agencies have provided Toxikon a unique understanding of product development and regulatory needs. With our vast knowledge of ASTM, AAMI, FDA, ICH, ISO, JP, and USP, we work with you to navigate the regulatory landscape to achieve your development goals.

Toxikon's microbiology capabilities include evaluations for:

  • Bioburden
  • Endotoxin
  • Sterility
  • Package integrity
  • Shelf life / Life cycle
  • Microbial identification
  • Compendial testing
  • Antimicrobial challenge
  • Cleaning validation
  • Customized microbial assessments


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Microbiology Testing Services | Bioburden | Sterility | Package Integrity | Microbial Identification | Shelf Life | Life Cycle | Compedia Testing | Cleaning Validation
In Vitro Efficacy, In Vitro Pharmacokinetics, In Vitro Pharmacology, In Vitro Studies, In Vitro Study Pharmacokinetics
Toxikon provides a range of in vitro efficacy services to support analytical and bioanalytical studies for pharmaceutical product development. Our in vitro pharmacology services involve binding assays, cell culture based assays and Microbiology/Virology studies.