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crotoxpath.com

CroToxPath

Nonclinical Drug development and Safety Evaluation. Providing safety evaluation and monitoring of toxicological studies on human and veterinary medicines, chemicals, agro-chemical products and food additives in accordance with their respective regulations. US, Canada, EU Regulatory Affairs Services. A Consortium of Experts. A consortium of highly qualified and experienced consultants in toxicology, nonclinical safety, pathology and regulatory sciences. In addition, we also offer a pathology peer review w...

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CroToxPath | crotoxpath.com Reviews
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Nonclinical Drug development and Safety Evaluation. Providing safety evaluation and monitoring of toxicological studies on human and veterinary medicines, chemicals, agro-chemical products and food additives in accordance with their respective regulations. US, Canada, EU Regulatory Affairs Services. A Consortium of Experts. A consortium of highly qualified and experienced consultants in toxicology, nonclinical safety, pathology and regulatory sciences. In addition, we also offer a pathology peer review w...
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CroToxPath | crotoxpath.com Reviews

https://crotoxpath.com

Nonclinical Drug development and Safety Evaluation. Providing safety evaluation and monitoring of toxicological studies on human and veterinary medicines, chemicals, agro-chemical products and food additives in accordance with their respective regulations. US, Canada, EU Regulatory Affairs Services. A Consortium of Experts. A consortium of highly qualified and experienced consultants in toxicology, nonclinical safety, pathology and regulatory sciences. In addition, we also offer a pathology peer review w...

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1

Chemical & Agrochemical Consulting

http://www.crotoxpath.com/index.php/consulting-services/chemical-agrochemical-consulting

Chemical and Agrochemical Consulting. CroToxPath’s team can help you to identify Toxicology studies needed for regulatory submissions to the US EPA (under TSCA and FIFRA regulations), using OPPTS guidelines, or for the submission under Canadian New Substance Notification Regulations and the European REACH program. We can write the protocols, identify a cost-effective CRO to conduct the studies, and help in the interpretation of the results and deal with any unsolved issues.

2

Resources

http://www.crotoxpath.com/index.php/resources

FDA Drugs Guidance Documents. The Freedom of Information Act (FOIA). SR&EDs Tax Incentive Program.

3

Scientific Research & Experimental Development

http://www.crotoxpath.com/index.php/consulting-services/sr-eds-education

Scientific Research and Experimental Development. CroToxPath can identify if your R&D program is eligible for the tax incentive program (Scientific Research and Experimental Development SR&EDs program), that is administered by the Canada Revenue Agency. Successful claimants can be eligible for cash refunds that we can claim through our accounting experts. For the eligible R&D research conducted in Canada we can prepare the technical / scientific portions of the claim.

4

Our Lead Scientists:

http://www.crotoxpath.com/index.php/lead-team

Ncluded in the external Scientific Experts Database for the Therapeutic Products Directorate of Health Canada, for the expert advice or review and recommendation on nonclinical and toxicology data. ACVP, the Society of Toxicologic Pathology, the American Society for Investigative Pathology, and the College of Veterinarians of Ontario.

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Nonclinical Drug development and Safety Evaluation. Providing safety evaluation and monitoring of toxicological studies on human and veterinary medicines, chemicals, agro-chemical products and food additives in accordance with their respective regulations. US, Canada, EU Regulatory Affairs Services. A Consortium of Experts. A consortium of highly qualified and experienced consultants in toxicology, nonclinical safety, pathology and regulatory sciences. In addition, we also offer a pathology peer review w...

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