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The Clinical Research Laboratories (CRL) is a great company! I had the opportunity to work with them on a recent project and I was impressed with their professionalism and dedication. The team at CRL is extremely knowledgeable and they go above and beyond to deliver high-quality results. I highly recommend CRL for any research needs.
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Clinical Research Laboratories: Your Partner in Quality and Innovation
Clinical Research Laboratories (CRL) is a leading contract research organization (CRO) that provides comprehensive services to the pharmaceutical, biotechnology, medical device, and consumer healthcare industries. With over 25 years of experience in clinical research, CRL has established itself as a trusted partner for companies seeking high-quality data and innovative solutions.
At CRL, we understand the challenges faced by our clients in bringing new products to market. That's why we offer a full range of services designed to support every stage of the product development process. From preclinical testing to post-marketing surveillance, our team of experts is dedicated to delivering accurate and timely results that meet regulatory requirements.
Our Services
Preclinical Testing: Our preclinical testing services include safety pharmacology studies, toxicology studies, and efficacy studies using animal models. We have state-of-the-art facilities equipped with the latest technology for conducting these studies.
Clinical Trials: We conduct Phase I-IV clinical trials across multiple therapeutic areas including oncology, cardiology, neurology, infectious diseases and more. Our experienced clinical operations team ensures that trials are conducted efficiently while maintaining patient safety.
Bioanalytical Services: We offer bioanalytical method development/validation/transfer services for small molecules/biologics/biosimilars/vaccines using LC-MS/MS or ELISA platforms. Our bioanalytical lab is GLP-compliant with state-of-the-art equipment.
Central Laboratory Services: Our central laboratory offers a wide range of testing services including hematology/oncology assays; chemistry assays; microbiology assays; immunogenicity assays; biomarker analysis etc., all performed under strict quality control measures.
Medical Writing & Regulatory Affairs: Our medical writing team provides high-quality documents such as protocols/amendments/ICFs/Clinical Study Reports (CSRs)/regulatory submissions etc., while our regulatory affairs team helps clients navigate complex regulatory requirements across different regions/countries.
Post-Marketing Surveillance & Pharmacovigilance: We provide post-marketing surveillance activities such as adverse event reporting/signal detection/risk management plans etc., along with pharmacovigilance activities such as literature search/safety database management etc., ensuring compliance with global regulations/guidelines.
Why Choose CRL?
Quality Assurance & Compliance - At CRL we follow strict quality assurance procedures throughout all stages of study conduct ensuring compliance with global regulations/guidelines like FDA/EMA/MHRA/TGA etc.
Expertise - With over 25 years' experience in clinical research across multiple therapeutic areas we have developed expertise which enables us to deliver high-quality data on time.
Innovation - At CRL we are committed to innovation through investment in new technologies/methodologies which enable us to deliver better results faster.
Customer Focus - At CRL customer satisfaction is at the heart of everything we do. We work closely with our clients throughout each project ensuring their needs are met at every stage.
Conclusion
If you're looking for a reliable partner who can help you bring your products from concept through commercialization then look no further than Clinical Research Laboratories. With our comprehensive range of services delivered by an experienced team committed to quality and innovation you can be confident that your project will be completed on time within budget whilst meeting all regulatory requirements/guidelines. Contact us today!
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