About Covance - Central Labs
Covance - Central Labs: Advancing Health through Comprehensive Drug Development Services
Labcorp Drug Development, formerly known as Covance, is a leading global contract research organization (CRO) that provides comprehensive drug development services to pharmaceutical and biotechnology companies. With a mission to improve health and lives, Covance has supported the development of the top 50 pharmaceutical drugs on the market.
As a full-service CRO, Covance offers nonclinical, preclinical, clinical, commercialization and regulatory consulting services to support drug development from discovery to post-market approval. The company's expertise in drug development spans across various therapeutic areas including oncology, neuroscience, infectious diseases and more.
Nonclinical Services
Covance's nonclinical services include toxicology studies that evaluate the safety of potential new drugs in animal models. These studies are conducted in compliance with international regulatory guidelines such as Good Laboratory Practice (GLP) regulations. The company also offers bioanalytical services that measure drug concentrations in biological matrices such as blood or urine.
Preclinical Services
In preclinical studies, Covance evaluates the efficacy of potential new drugs using disease models that mimic human conditions. These studies help identify promising candidates for further testing in clinical trials. Preclinical services also include pharmacokinetic and pharmacodynamic evaluations which assess how drugs are absorbed, distributed and eliminated by the body.
Clinical Services
Covance's clinical services encompass all phases of clinical trials from Phase I to IV. Phase I trials involve testing new drugs for safety in healthy volunteers while Phase II-IV trials evaluate efficacy and safety in patients with specific diseases or conditions. Clinical trial management includes site selection and monitoring activities as well as data management and statistical analysis.
Commercialization Services
Once a drug has been approved by regulatory agencies such as FDA or EMA for marketing authorization; it enters into commercialization phase where it is manufactured at large scale for distribution worldwide.Covances' Commercialization team helps clients navigate this process by providing strategic planning support along with manufacturing oversight & quality control measures ensuring timely delivery of high-quality products.
Regulatory Consulting
Regulatory consulting is an essential component of successful drug development programs.Covances' Regulatory Consulting team provides guidance on navigating complex regulatory requirements across different geographies.Their experts have extensive experience working with global regulatory authorities including FDA ,EMA etc.,and can provide valuable insights into developing strategies for successful product registration & approval processes.
Conclusion:
In conclusion,Covance - Central Labs is an industry leader when it comes to providing comprehensive drug development solutions.With their vast experience spanning over decades they have helped numerous clients bring life-saving therapies from bench-to-bedside.They offer end-to-end solutions starting from early-stage research through commercialisation while ensuring compliance with international regulations throughout every step of the process.If you're looking for a reliable partner who can help you advance your healthcare innovations,Covance should be your first choice!
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