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Frequently Asked Questions

1. What does Toxikon do?
2. Is Toxikon FDA registered?
3. Can Toxikon perform GLP compliant studies?
4. What are Toxikon's registration numbers?
6. How do I start requesting testing services?
7. How do I request protocols?
9. What  does Toxikon manufacture?  
10. When will testing begin?


Answers

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.
5. Toxikon's corporate office is located at 15 Wiggins Avenue, Bedford, MA 01730.
Click for directions to this facility
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.