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Be Agilent Sure with your UV-Vis and FTIR analysis in Pharma and Biopharma

安捷伦 | Be Agilent sure
BE AGILENT SURE - With your UV-Vis and FTIR analysis in pharma and biopharma

Improve your method development and QA/QC workflow

Today’s drug development and manufacturing processes require efficiency, safety, and controls that ensure high quality for active ingredients and finished dosage forms. Agilent offers a comprehensive range of accurate, innovative, and compliant molecular spectroscopy solutions that deliver all the performance you need in your pharma and biopharma laboratories.

  • Reduce sample handling, save time, and make measurements faster and easier with Agilent’s UV-Vis and FTIR instruments—vital for testing incoming raw materials, small molecule APIs or other drug components
  • Perform non-destructive sample measurements to investigate protein stability and structure
  • Recover samples for further analysis by other techniques such as HPLC and MS
  • Conduct comparability studies, like Biosimilars analysis
  • Utilize Agilent tools during formulation development
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Agilent CrossLab Compliance

Address the regulatory requirements of both 21 CFR Part 11 and EU Annex 11 with confidence. Agilent’s CrossLab qualification services are available for both software and hardware to reduce regulatory risk, meet global compliance—including the latest US pharmacopeia—and deliver peace of mind.

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Molecular Spectroscopy Analysis in Drug Development and QA/QC

Dr. Kevin Grant
Product Manager, Agilent Technologies

Learn how Agilent’s molecular spectroscopy solutions can be used to improve productivity as well as provide other benefits associated with reduced sample handling. Use these tools to streamline your analysis in drug development and QA/QC with products designed for regulated environments.

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Monoclonal Antibody Structure using Cary 8454 UV-Vis

Ursula Tems
Product Manager, Agilent Technologies

See how the Cary 8454 UV-Vis is used during formulation and development to provide valuable information about monoclonal antibody structure. Learn why UV-Vis is an ideal analytical tool to sit beside liquid chromatography or mass spec instrumentation in biopharmaceutical development.

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Using a Diode Array UV-Vis in Regulated Environments

Ursula Tems
Product Manager, Agilent Technologies

See how the Cary 8454 UV-Vis is optimized for today’s laboratory, with benefits for workflow and productivity with proven PDA technology. Learn how the Cary 8454 UV-Vis will help meet your compliance needs.

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Agilent’s range of molecular spectroscopy systems provide solutions
for your analytical and compliance needs

Cary 8454 UV-Vis

The Cary 8454 UV-Vis diode array spectrophotometer delivers the full spectrum with each measurement for rapid, complete spectral QA/QC analysis of your samples. The UV-Visible ChemStation software provides sophisticated method development capabilities, including measurement sequence automations, single and multi-component analysis, and compatibility with Agilent’s OpenLAB ECM software solution for efficient laboratory-wide data storage and protection.

Cary 630 FTIR

The Cary 630 FTIR has innovative sampling technologies that eliminate the tedious sample preparation requirements typical for traditional FTIR. Never load or clean a transmission cell again with the Cary 630 Dialpath, TumblIR and ATR accessory range. They are suitable for liquids, pastes, gels, and solid samples; as well as ideal for everyday use in multiuser environments for QA/QC laboratories.

Innovative molecular spectroscopy solutions that deliver performance, reliability, and compliance

Cary 8454 UV-Vis Demo

Cary 8454 UV-Vis Demo Video

See how the software and hardware capabilities of the Cary 8454 UV-Vis simplify your workflow, increase productivity, and give accurate answers fast.

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Cary 60 UV-Vis Demo

Cary 60 UV-Vis Demo Video

Learn how the Cary 60 UV-Vis offers the lowest cost of ownership and lets you measure precious samples (microvolumes) with ease.

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Cary 630 FTIR Demo

Cary 630 FTIR Demo Video

See the Cary 630 FTIR in action and learn how its unique hardware and software features can simplify your workflow, increase productivity, and give accurate answers every time.

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Complete your pharma and biopharma workflow

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部件和备件

Agilent Certified Reference Materials (CRMs) offer a convenient way for you to collect evidence that your UV-Vis is working to specification and is fit-for-purpose. Ideal for analysts who need to conform to ISO 9001, GLP, GMP, and other international and regulatory standards like USP and EP.

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OpenLab ECM Software

OpenLAB ECM Software

OpenLAB ECM is the most comprehensive solution for storing, accessing, and protecting the data that you get from your Cary 8454 UV-Vis. It is the tool of choice for many of the top pharma companies because it helps satisfy the ALCOA+ standards of data integrity set by US FDA 21 CFR Part 11 and EU Annex 11.

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CrossLab 标志

Agilent CrossLab

Trust Agilent CrossLab service experts to deliver valuable insights and keep your instruments running at top performance. Our industry-leading services—tailored to meet your needs—include application consulting, repairs, preventive maintenance, compliance verification, and education. Ask us how we can support your laboratory today.

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