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Life Sciences & Diagnostics and Analytical & Enterprise Solutions

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We are now two standalone organizations

  • Life Sciences & Diagnostics

    A Life Sciences and Diagnostics business focused on enabling scientists and healthcare professionals to advance research, discovery and detection to improve global health

  • Analytical & Enterprise Solutions

    An Analytical and Enterprise solutions business, including leading OneSource laboratory services, focused on accelerating scientific outcomes

Pharmaceuticals QA/QC | 爱游戏平台注册登录 - 爱游戏登录网,爱游戏平台注册登录
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Pharmaceuticals QA/QC

When it comes to QA/QC, we offer everything to stay compliant each step of the way, from our analytical instrumentation to our unique OneSource service and support. When these tools come together, they work as a system to create safe, quality products consumers can trust and pharmaceutical manufacturers can feel confident about.

Good Manufacturing Practice (GMP) not only drives the QA/QC inside your company, but it also guides 爱游戏平台注册登录 ’s development of the technologies, tools and processes we build to assure you are meeting your regulatory obligations while you continuously manufacture compliant product.

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Regulatory & Compliance

Helping our customers meet compliance in a regulated environment

Given today’s evolving and increasingly complex regulatory environments, a whole new mindset to auditing, moving away from traditional instrument validation approaches and concentrating on the data lifecycle to detect gaps or fraud in product development and quality control are critical to compliance.

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Drug Substance & Excipients

Ensuring purity & assuring compliance

In order to comply with GMP standards, including identification of incoming raw material testing, drug substance assay and excipient quality, you need the latest analytical tools and data to meet compliance.

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Drug Product

Mitigating risk while maximizing production

Drug product or finished dosage form (tablet, capsule, injectables) contains a drug substance and excipient. All drug products must be GMP compliant to be released for commercial use. 爱游戏平台注册登录 provides the tools you need to release safe and effective medicines giving the peace of mind you need when it comes to audits.

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Control of Impurities

Keeping impurities and compliance under control

The control of impurities is mandatory for both drug substance and drug product testing. QA/QC laboratories need to guarantee impurity levels are below the threshold established by regulatory authorities such as FDA, EMA, MHRA to ensure GMP compliance.

At 爱游戏平台注册登录 , we provide the tools you need for you to take control of your impurities testing.

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Stability Testing

Monitoring and measurement for shelf-life and storage

Typically, both drug substance and drug product are tested in at least two different storage conditions: long term ambient storage temperature and accelerated conditions predicting product stability at a long period of time.

To highlight its importance, ICH provides a dedicated section to Stability - at 爱游戏平台注册登录 , we provide the tools you need so you have your shelf-life and storage temperature under control.

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Explore Our Solutions

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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Elemental Impurities Testing

Elemental Impurities in drug products can arise from several sources, including interactions with processing equipment or container/closure systems, presence in ...

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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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Pharmaceutical Raw Material Identification

The analysis of all incoming pharmaceutical raw materials is a key part of GMP compliance to guarantee safety and efficacy of a finished dosage form which is la ...

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Drug Substance Assay

Inspections of drug substances are designed to confirm manufacturing plants, as well as the quality control laboratory, follow CGMP regulations. An extensive se ...

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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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Excipients Characterization

The quality of excipients is extremely important since 90% of medicines are made up of them. When it comes to regulatory guidelines, there are several the indus ...

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Residual Solvents

The synthesis of active pharmaceutical ingredients (API) may require multiple reaction steps that produce undesirable reaction byproducts or utilize various sol ...

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Explore Our Instruments

Chromatography

Whatever your application, industry requirements or regulations, we have a breadth of solutions designed to solve your separation and detection challenges. Our ...

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Atomic Spectroscopy

If you're looking for proven AA, ICP-OES, ICP-MS, or mercury analysis systems, you've come to the right place. 爱游戏平台注册登录 has been at the forefront of atomic s ...

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Molecular Spectroscopy

Today’s advanced and increasingly diverse Advanced Materials laboratories are facing new challenges daily – starting from raw materials right up to the finished ...

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Thermal Analysis

Improve accuracy, sensitivity, and performance using our comprehensive portfolio of instruments in Differential Scanning Calorimetry (DSC), Thermogravimetric An ...

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