Our diverse clients are developing cures and remedies in these industries
![Laboratory technician examining samples under a microscope with lab equipment under Good Laboratory to generate data and safety documentation for nonclinical / preclinical studies. Biotechnology written under image.](/web/image/2273-13417cb6/Edit%202.png)
Biotechnology
![Pharmacokinetic, toxicology and safety pharmacology preclinical studies conducted under Good Laboratory Practice enable the development of remedies. Pharmaceutical written under image.](/web/image/2274-b6a3999d/Website%20image%20edit%201.png)
Pharmaceutical
![Healthy pets (cat and dog) with scientist after cures produces from preclinical research studies including pharmacokinetics, safety pharmacology and toxicology](/web/image/2275-013e976d/Website%20image%202.png)
Animal Health
![Scientist using advanced technology to assist in preclinical research for agricultural purposes. Agrochemical written image](/web/image/2276-aa3d0d9a/Edit%203.png)
Agrochemical
Our Solutions
![Preclinical pharmacokinetic assessment showing separation of plasma from red blood cells as a result of nonclinical research studies from in vivo test systems](/web/image/1595-e6148018/ATS-blog-thumb_2020-10-A_HTPF-PK-Screening.jpg)
Pharmacokinetics
Knowledge of the fate (Absorption, Distribution, Metabolism, Elimination) of a test substance is necessary to predict its action on a test subject . With Attentive, you have at your disposal a wide range of in-vivo test systems as well as protocols and reporting infrastructure to ensure you receive quality data in a timely manner to select the best test substance and doses for your programs. Attentive Scientists bring the experience necessary to excel at executing these studies to assist you by performing in-vivo studies during the discovery and lead optimization phases of your research
![A drug capsule with side effects written on it to show how Attentive nonclinical / preclinical toxicology studies help evaluate risk relative to safety for pharmaceutical development and prevent adverse effects](/web/image/1596-94053605/ATS-blog-thumb_2021-05-A_CNS-Safety-Pharma.jpg)
Toxicology
Regulatory toxicology studies to evaluate the relationship between various doses of your drug molecule and adverse events require close collaboration between scientists with multiple levels of expertise from the development company and the contract research organization (CRO). Attentive’s processes ensure transparent communication, collaboration and dialogue that will keep up with your ever-changing needs for lead optimization, candidate selection as well as regulatory-enabling studies
![The Attentive Science safety pharmacologist combining knowledge from Physiology, Pharmacology and Toxicology to evaluate effects on the electrocardiogram (ECG), with particular emphasis on ventricular depolarization repolarization, as well as any potential effects on blood pressure (BP) and heart rate (HR).](/web/image/1599-90a9d4e2/Safey%20Pharm%201.png)
Safety Pharmacology
Safety Pharmacology studies are designed to detect the potential undesirable pharmacodynamic effects of new chemical entities on physiological functions in relation to exposure in the therapeutic range and above. In addition to you obtaining scientifically robust data, you have access to a vast network of experts at Attentive
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