Charles River Laboratories

NYSE CRL

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Charles River Laboratories EV to Free Cash Flow Ratio (EV/FCF) on June 03, 2024: 31.52

Charles River Laboratories EV to Free Cash Flow Ratio (EV/FCF) is 31.52 on June 03, 2024, a -31.77% change year over year. The EV/Free Cash Flow ratio compares a company's enterprise value to its free cash flow. It provides insight into the company's valuation relative to its ability to generate cash flow after accounting for capital expenditures. A lower ratio suggests a potentially more favorable valuation.
  • Charles River Laboratories 52-week high EV to Free Cash Flow Ratio (EV/FCF) is 48.50 on August 10, 2023, which is 53.88% above the current EV to Free Cash Flow Ratio (EV/FCF).
  • Charles River Laboratories 52-week low EV to Free Cash Flow Ratio (EV/FCF) is 30.41 on October 30, 2023, which is -3.52% below the current EV to Free Cash Flow Ratio (EV/FCF).
  • Charles River Laboratories average EV to Free Cash Flow Ratio (EV/FCF) for the last 52 weeks is 40.75.
NYSE: CRL

Charles River Laboratories

CEO Mr. James C. Foster J.D.
IPO Date June 23, 2000
Location United States
Headquarters 251 Ballardvale Street, Wilmington, MA, United States, 01887
Employees 20,400
Sector Healthcare
Industry Diagnostics & research
Description

Charles River Laboratories International, Inc. provides drug discovery, non-clinical development, and safety testing services in the United States, Europe, Canada, the Asia Pacific, and internationally. It operates through three segments: Research Models and Services (RMS), Discovery and Safety Assessment (DSA), and Manufacturing Solutions (Manufacturing). The RMS segment produces and sells rodents, and purpose-bred rats and mice for use by researchers. This segment also provides a range of services to assist its clients in supporting the use of research models in research and screening pre-clinical drug candidates, including research models, genetically engineered models and services, insourcing solutions, and research animal diagnostic services. The DSA segment offers early and in vivo discovery services for the identification and validation of novel targets, chemical compounds, and antibodies through delivery of preclinical drug and therapeutic candidates ready for safety assessment; and safety assessment services, such as toxicology, pathology, safety pharmacology, bioanalysis, drug metabolism, and pharmacokinetics services. The Manufacturing segment provides in vitro methods for conventional and rapid quality control testing of sterile and non-sterile pharmaceuticals and consumer products. This segment also offers specialized testing of biologics that are outsourced by pharmaceutical and biotechnology companies. It also provides contract vivarium operation services to biopharmaceutical clients. The company was founded in 1947 and is headquartered in Wilmington, Massachusetts.

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StockViz Staff

September 19, 2024

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