testing by product category
biotechnology
drug discovery & development
manufactured products

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testing by product category

For easy of use, we have grouped our Biopharmaceutical Services offerings under the different category headings listed below:

Biotechnology
Drug Discovery & Development
Manufactured Products including Medical Devices

biopharmaceutical product develoment, biopharmaceutical testing services Biopharmaceutical Testing by Product Category | Charles River Charles River Biopharmaceutical Services provides clients with over twenty years of experience developing customized testing and manufacturing packages addressing the specific regulatory requirements through each step of the development of your product.

Charles River and WuXi AppTec to Combine

For more information please call:

+44 (0) 1875 614545
askcharlesriver@crl.com

RELATED INFO

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Biopharmaceutical Services Overview

Webinar Replay: Viral Safety Assessment of Biopharmaceuticals

This webinar focused on the regulatory requirements for viral clearance studies as well as the influence of various other factors relevant to designing these studies.

NewLab BioQuality AG Website

Charles River has acquired NewLab BioQuality, a German-based service company providing GLP/GMP-compliant solutions for the quality control of biopharmaceuticals.

News & Events

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juil. 13 - New Genetic Toxicology Assays wi...

juin 09 - Expanded Immunogenicity Testing i...

sept. 03-sept. 04 - Asahikawa, Hokkaido, Japan - Japanese Association for Experimental ...

sept. 13-sept. 15 - San Diego, CA - Annual Biotech Symposium on Biotechnology-Derived T...

août 24-août 27 - South Carolina, USA - Charles River LAL Workshop

Related Jobs

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Clinical Pathology Analyst Tranent, Scotl...

Health & Safety Officer Tranent, Scotland

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Biopharmaceutical Services Overview

Webinar Replay: Viral Safety Assessment of Biopharmaceuticals

This webinar focused on the regulatory requirements for viral clearance studies as well as the influence of various other factors relevant to designing these studies.

NewLab BioQuality AG Website

Charles River has acquired NewLab BioQuality, a German-based service company providing GLP/GMP-compliant solutions for the quality control of biopharmaceuticals.

Biopharmaceutical Services Literature

juil. 13

New Genetic Toxicology Assays with Low Compound Requirements

Genetic toxicology testing is a key element in the development of pharmaceuticals, agrochemicals and chemicals. Formal GLP testing is required as part of the safety evaluation of all compounds; however, many companies perform non-GLP screening genetox tests very early to avoid expensive failures later. At this point, compound availability is normally very limited, so it is important to minimize usage while ensuring the most accurate predictivity of the outcome of the eventual GLP assays. Charles River now offers in vitro genetic toxicology screening assays where compound requirements may be as little as 10 mg: Bluescreen HC and Bluescreen HC S9 and µAmes.

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juin 09

Expanded Immunogenicity Testing in Biologics Now Offered

Charles River Biopharmaceutical Services (BPS) has experience developing, validating and implementing in vivo, in vitro and ex vivo assays to study immunogenicity and biological potency. To address the evolving needs of our customers, we are expanding our existing immunogenicity portfolio of in vivo immunopotency assays, ELISAs and cell-based assays to include cell-based neutralizing assays. Cell-based neutralizing assays can be used to detect the presence of anti-drug antibodies that can interfere with the drugs’ effectiveness, an important consideration in immunogenicity risk assessment.

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sept. 03–sept. 04

Japanese Association for Experimental Animal Technologists (JAEAT) Annual Meeting Asahikawa, Hokkaido, Japan

Charles River will be exhibiting at this event. At this meeting the latest issues being faced by those in the field of laboratory animal technology will be discussed, and attendees will have the opportunity to exchange their views on these issues. Our Research Models and Services group is committed to providing you with the critical resources needed to advance your research, with a focus on responsive customer service and leadership in veterinary science. Please stop by our booth to learn why you can trust us to be an integral part of your research programs – now and in the future.

sept. 13–sept. 15

Annual Biotech Symposium on Biotechnology-Derived Therapeutics San Diego, CA

The Biotech symposium is designed to provide insights into nonclinical development of biologics, Specific topics that will be covered include: Safety Pharmacology of Therapeutic Proteins; Impact of Immunomodulatory Agents on Host Resistance; New Paradigms for Predicting Cancer Risks Posed by Immunosuppressive Drugs; PK/PD Modeling: Extrapolating from Animal Data into First-in-Human Dose; and DART Programs for Biotherapeutics: Study Designs, Challenges and Regulatory Influences. In addition to the symposium, we will offer a workshop on endemic diseases and micro-flora as they relate to toxicology on September 12th.

août 24–août 27

Charles River LAL Workshop South Carolina, USA

This workshop offers basic information, including an introduction to gel and kinetic methodologies, compendia and regulatory updates, sources and solutions for LAL test interference, gel-clot and kinetic product validations, and other topics.

Clinical Pathology Analyst: Tranent, Scotland

The Clinical Pathology Analyst is responsible for undertaking routine and specialised analyses in clinical chemistry and haematology as well as for assessing and reporting clinical pathology data. Other tasks include monitoring the performance of assays and equipment with internal and external quality control, maintaining legible and permanent records of all results obtained together with relevant supporting data, and participating in development of new techniques and services.

Health & Safety Officer: Tranent, Scotland

The Health & Safety Officer provides support to the Safety Manager in all matters relating to the provision of H&S. Major responsibilities of this position include: providing assistance to local managers with assessments and other practical requirements as necessary under H&S legislation; assisting in the operation, development and organisation of safety and health monitoring schemes; assisting in the development and monitoring of systems for the control of all operations involving the use of radioactive materials in accordance with current legislation; undertaking incident investigations as necessary; serving as a liaison with the Occupation Health Service and internal and external Enforcing Authorities as required; carrying out regular H&S audits; and assisting in staff safety training.

Charles River Laboratories, Inc.