ATRPL Testing and Research offers an array of NABL and non-NABL Preclinical toxicology studies to its customers. The studies, in which our Toxicology services team has expertise, are composed of acute, sub-acute, and sub-chronic studies in various test systems with different routes of administration, along with in-vitro/in-vivo genotoxicity studies. These studies are performed in compliance with global regulatory guidelines, ISO, USP, IP, EP OECD, etc. at ATRPL in India.

We provide a comprehensive range of toxicology and safety pharmacology services by international regulatory guidelines.  Phase, we assist in toxicological safety assessment to identify and eliminate the unsafe elements at the earliest stage in drug development with routine screening of compounds in the R&D.

ATRPL has the latest facilities to evaluate the different products in a professional manner that results in the timely delivery of the reports. The rich experience of our scientific team helps our customers meet their specific preclinical and other early-stage product development needs, enhance their decision-making process, and save their time and resources.