Toxikon showcasing preclinical testing services at DeviceTalks Boston

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ToxikonToxikon is a preclinical Contract Research Organization (CRO) located in an FDA registered and ISO 17025 accredited laboratory facility in Bedford, Mass., and a second European lab operation in Leuven, Belgium. The company contracts and partners with biotech, pharmaceutical and medical device industries to deliver product development services from concept to final product. Its professional and scientific staff is experienced in a comprehensive range of compound structures, therapeutic agents, and medical devices, including combinations products.

Featured services:

  • ISO 10993 biocompatibility safety studies (GLP)
  • Preclinical early efficacy and surgical research
  • Chemical characterization/extractables and leachables
  • Cleaning, disinfection and sterilization validations

Visit Toxikon at booth #202 at DeviceTalks Boston.

(Learn from some of the medical device industry’s top executives and experts at DeviceTalks Boston on Oct. 2.)

DeviceTalks West: Expertise you need to know

textadimage Medical device suppliers are light years away from the days when they merely filled orders to spec for medtech OEMs – as a visit to the upcoming DeviceTalks West will quickly confirm.

From incorporating steerability into catheters to getting validation and testing done right, the companies serving the medical device industry have become specialized experts in their own right.

Read on to discover five example of medical device expertise to be had at DeviceTalks West, which runs Dec. 11–12 in Orange County, Calif.

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