About us
About the Company
Pretox Consultancy (PTC) is a specialized consulting organization dedicated to delivering independent, high-quality, and cost-effective guidance in the field of preclinical / nonclinical research and development.
We provide independent expert guidance about different type of industries/segments such as pharmaceuticals industries, agricultural industries, medical device, risk assessment, impurities assessment, clinical pathological aspect and histopathological evaluation including peer review pathology. We support clients at every stage of their product development — from early nonclinical planning and study design to data interpretation and regulatory submissions.
We work closely with Contract Research Organizations (CROs) to ensure studies are executed according to Good Laboratory Practice (GLP) and meet global standards set by OECD, NDCT Rules, ICH, EMA, and FDA.
We are knowledgeable and experienced in monitoring the entire process of conducting preclinical studies in various animals—such as rats, guinea pigs, mice, rabbits and dogs by common and uncommon routes.
Our expertise in small molecule, large molecule, biosimilar, vaccine, excipient, extractable, leachable, generic products, agriproducts, complex formulations etc. – Development strategy in preclinical aspect.
We have qualified CROs to meet Sponsor needs and ensure satisfaction:
Personally visited to CRO and interacted with TFM and scientific team to understand/evaluate the depth knowledge to conduct the preclinical toxicity studies.
Cost effective selection of preclinical CROs with maintain the GLP compliance norms.
Negotiates reasonable timelines with stakeholders and sets acceptable priorities.
Align the CROs to ensure a smoother and more efficient process