1. Toxikon Corporation is a contract research organization that performs compliance studies for product safety.
Click for more information |
| 2. Toxikon is FDA registered and ISO 17025 accredited. |
| 3. Yes. Toxikon's capabilities include performing studies in compliance with US FDA 21 CFR Part 58. Toxikon also performs GMP studies in compliance with US FDA 21 CFR Part 820. |
| 4. Contact Regulatory Affairs Department at 800.458.4141. |
|
|
| 6. Send completed test requisition form(s), protocols (if applicable), and test article(s) to the attention of Toxicology Login at 15 Wiggins Avenue, Bedford, MA 01730 |
7. Contact your Account Manager or Client Services representative.
To check the Account Manager in your area, click here |
8. Test requisition forms may be accessed from the "Resource Center" link.
|
| 9. Toxikon Corporation does not manufacture any products. |
| 10. Testing will be scheduled as soon as the samples arrive and all the related paperwork is completed. |
| 11. Send e-mail to mis@toxikon.com with complete contact information requesting an account in the sample management system |
