Covance Preclinical Services

サービス

前臨床

Plan your next preclinical study or partner with us for an IND/CTA-enabling package to get you from research to clinical trials faster. Save up to 30% on your preclinical timeline.

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DISEASE MODELS

Oncology Models and Cell Lines

In vitro および In vivo ファーマコロジー有効性モデル、in vivo 画像化技術、さらに焦点放射線機能を含む包括的な臨床前オンコロジー研究により、お客様の臨床前オンコロジー化合物を提案します。

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ADMINISTRATION ROUTE

Inhalation Testing Capabilities

Inhalation toxicology studies are becoming vital in assessing the safety and potential toxicity of inhaled drugs or chemicals as respiratory diseases including asthma, chronic obstructive pulmonary disease (COPD) and cystic fibrosis (CF) become more common.

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PROGRAMMATIC DEVELOPMENT

IND/CTA-Enabling Packages

Accelerate your molecule's success with Early Phase Development solutions that help to advance your molecule swiftly through critical milestones while maximizing the asset's value. 初期の医薬品開発のタイムラインを 30% 縮めましょう。

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MARKETPLACE

Find the Right Partner

お客様の資産の可能性実現を支援する熱意とリソースを持った理想的なパートナーを見つけてください。当社のプライベートで安全な専用オンラインポータルを通じて、お客様は潜在的な投資家やパートナーとお客様の資産に関する情報を共有することができます。 It's one more innovative way to transform your program.

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Preclinical Facilities & Locations

Enjoy global support and capacity for your preclinical studies with labs strategically positioned around the world. View all facilities

Covance Pre-Clinical Solutions

Unleash the Power of Connected Insights

The landscape of development is becoming more complex. You still need your studies delivered on-time and on-budget.

By connecting inspiring science with data, our committed scientific teams uncover insights from preclinical and clinical studies to help you reach your development milestones.

数字で見るメリット

Preclinical supported

81%

of the FDA's 2019 NDA/BLA drugs

Preclinical supported

77%

of the FDA's 2019 biologics

Save up to

30%

on your preclinical timeline

More than

125

billion SEND data points submitted

Have Questions?

ご利用者の声

“A dependable and reliable source for complicated studies with dedicated and extremely competent study direction.” –Project leader from a global pharmaceutical company

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