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Drug Product

Mitigating risk while maximizing production

Drug product or finished dosage form (tablet, capsule, injectables) contain a drug substance (API) and excipients. All drug products must be GMP compliant to be released for commercial use.

The suitability of a drug product for its intended use is defined by attributes such as the identity, strength, and purity – which can be achieved by using instruments, consumables and services you can find from 爱游戏平台注册登录 .

Our analytical instrumentation, informatics solutions, and service and support, provide pharmaceutical manufacturers confidence in the quality of their product and compliance in their process from beginning to end.

  • Analytical Solutions for Vaccines: Quality in Every Dose

Analytical Solutions for Vaccines: Quality in Every Dose

In the race for swift vaccine development, the tireless efforts behind bringing these life-saving solutions from labs to clinics often fade into the background. With vaccines preventing over 20 diseases and averting up to 5 million deaths annually, they've been champions in extending and improving lives. From historical successes to the promising future of therapeutic vaccines, the journey demands rigorous testing.

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Resources

Direct Trace-Element Analysis in Cell Culture Media and Raw Materials with the NexION 5000 ICP-MS

Raw material preparation and formulation is a known source of elemental content and variation in cell culture media. Other sources of trace metal concentrations ...

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Effects of Ionizable and Non-ionizable Excipients on Lyophilized RNA Formulations Using FTIR-ATR Technology

There are ongoing attempts to improve the storage stability of mRNA vaccines by converting them to solid forms using various drying methods. Lyophilization is o ...

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Accurate RNA quantification using microvolume cuvettes and the LAMBDA 365+ UV/Vis spectrometer

UV/Vis spectrometers are highly versatile instruments employed in a wide variety of applications. The development of microvolume cuvettes that can be easily fit ...

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Explore Our Solutions

Extractables & Leachables

Pharmaceutical laboratories must evaluate the interactions between packaging material and formulation, applying risk assessments defined on ICH Q9 guidelines to ...

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Drug Product Assay

An extensive set of analytical testing and acceptance criteria is applicable to drug products –including universal and specific test criteria established by ICH ...

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Primary Packaging

GMP accredited labs check the quality of primary packaging containing drug products. The testing and qualification of plastic packaging systems and components f ...

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耗材及配件

Your partnership with 爱游戏平台注册登录 doesn't stop when you purchase an instrument. We also have a complete line of consumables and accessories engineered to keep t ...

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Dissolution Testing

Pharmaceutical labs consider dissolution testing to be one of the critical steps in the drug development process. It makes an impact at almost every step of the ...

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雜質分析

確保符合USP <232>/<233>和ICH Q3D要求(該標準製藥監管政策有史以來最重大的修訂)。 我們提供從樣品製備、儀器檢測的完整解決方案,確保完全符合USP <232> / <233>和ICH Q3D中的相關規定。

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Explore Our Instruments

色譜

無論您要麵對怎樣的的應用、技術和法規要求,我們都有色譜解決方案來解決您的分離和檢測難題。 我們的多元化產品組合包括液相色譜儀(LC),液相色譜/質譜聯用儀(LC/MS),氣相色譜儀(GC),氣相色譜/質譜聯用儀(GC/MS)和Arnel-GC工程色譜係統。此外,我們提供最全麵的樣品前處理技術解決方案,其中包括一係列的自 ...

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原子光譜

如果您正在尋找世界領先的AA,ICP-OES,ICP-MS或汞分析係統,您已經到了正確的地方。 全世界數以萬計的用戶依靠爱游戏平台注册登录 光譜儀快速、高效、輕鬆地從無機元素分析中獲得準確的結果。無論哪種領域、應用或樣品類型,我們都有相應的工具和專業知識可提供幫助 - 所有這些都是基於50多年來在原子光譜領域累積的前 ...

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AYX爱游戏app体育官方下载
複雜材料表征技術,總有一款適合您。我們擁有全麵的分析解決方案,可以為各種的實驗室提供理想的分子光譜儀器,包括紫外光譜,紅外光譜及熒光光譜。 更高精度,確保獲得更高的靈敏度 靈活的設計,滿足不同尺寸的樣品測試 多種采樣附件可供選擇 更短的樣品配置時間 軟件易學易用,提供專業的結果 作為紅外光譜技術的業界先驅,我們在60年 ...

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熱分析

使用我們全麵的熱分析儀器係列,提高熱分析的精確度,靈敏度和性能。我們業界領先技術的應用包括: QA/QC應用 藥物過程研究 聚合物研究 回收塑料的識別 包裝材料的測定 納米材料 塗料 複合材料 其他更多 僅供科學研究,非臨床診斷用途。

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