์ฃผ์š” ์ฝ˜ํ…์ธ ๋กœ ๊ฑด๋„ˆ๋›ฐ๊ธฐ

๊ท€ํ•˜์˜ ๋ธŒ๋ผ์šฐ์ €๊ฐ€ ์™„๋ฒฝํ•˜๊ฒŒ ์ง€์›๋˜์ง€ ์•Š์Šต๋‹ˆ๋‹ค. ์˜ต์…˜์ด ์žˆ๋Š” ๊ฒฝ์šฐ ์ตœ์‹  ๋ฒ„์ „์œผ๋กœ ์—…๊ทธ๋ ˆ์ด๋“œํ•˜๊ฑฐ๋‚˜ Mozilla Firefox, Microsoft Edge, Google Chrome ๋˜๋Š” Safari 14 ์ด์ƒ์„ ์‚ฌ์šฉํ•˜์„ธ์š”. ๊ฐ€๋Šฅํ•˜์ง€ ์•Š๊ฑฐ๋‚˜ ์ง€์›์ด ํ•„์š”ํ•œ ๊ฒฝ์šฐ ํ”ผ๋“œ๋ฐฑ์„ ๋ณด๋‚ด์ฃผ์„ธ์š”.

์ด ์ƒˆ๋กœ์šด ๊ฒฝํ—˜์— ๋Œ€ํ•œ ๊ท€ํ•˜์˜ ์˜๊ฒฌ์— ๊ฐ์‚ฌ๋“œ๋ฆฝ๋‹ˆ๋‹ค.์˜๊ฒฌ์„ ๋ง์”€ํ•ด ์ฃผ์„ธ์š”

Elsevier
์—˜์Šค๋น„์–ด์™€ ํ•จ๊ป˜ ์ถœํŒ

PharmaPendium์€ ๋” ๋‚˜์€ ์•ฝ๋ฌผ ๊ฒฐ๊ณผ๋ฅผ ์œ„ํ•ด ์•ฝ๋ฌผ ์•ˆ์ „์„ฑ ๋ฐ ํšจ๋Šฅ ๊ฒฐ์ •์„ ์ง€์›ํ•ฉ๋‹ˆ๋‹ค.

์ž์‹  ์žˆ๊ฒŒ ๋ฐœ๊ฒฌ, ํ˜์‹  ๋ฐ ๊ฐœ๋ฐœํ•˜๋ ค๋ฉด ๊ณ ํ’ˆ์งˆ ๋ฐ์ดํ„ฐ๊ฐ€ ํ•„์š”ํ•ฉ๋‹ˆ๋‹ค. PharmaPendium์€ ๋น„๊ตํ•  ์ˆ˜ ์—†๋Š” ๊ทœ์ œ ๋ฐ ์•ฝ๋ฌผ ๋ฐ์ดํ„ฐ๋ฅผ ์ „์ฒด ํ…์ŠคํŠธ ๊ฒ€์ƒ‰ ๋ฐ ์˜ˆ์ธก ๋„๊ตฌ์™€ ๊ฒฐํ•ฉํ•ฉ๋‹ˆ๋‹ค. PharmaPendium์œผ๋กœ ๋™๋ฌผ ์‹คํ—˜์„ ์ค„์ด๊ณ  ์•ฝ๋ฌผ์„ ๋” ๋น ๋ฅด๊ฒŒ ์ถœ์‹œํ•˜์‹ญ์‹œ์˜ค.

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FDA ๋ฐ ์„ธ๊ณ„ ์ตœ๊ณ ์˜ ์ œ์•ฝ ํšŒ์‚ฌ์—์„œ ์‚ฌ์šฉ

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To advance the best drug candidates, you want to prove better performance. PharmaPendium has user-friendly tools to help you analyze safety, deliverability and efficacy data.

  • Predict drug-drug interactions with confidence

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  • Access data with a translational view across preclinical, clinical and post-market, including:

    • Preclinical and clinical safety

    • Animal models

    • Adverse events (MedDRA)

    • Pharmacokinetic parameters

    • Metabolism and transport

    • Clinical trial and endpoints

    • Post-market reports (FAERS)

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  • Discover complete regulatory packages from the EMA and FDA, and FDA Advisory Committee Meeting Documents

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  • Rapidly respond to regulatory questions using comparative data from FDA/EMA drug approval and review documents

Analyze the toxicity of drug candidates and advance the 3Rs with the new Tox Navigator

Developed in collaboration with Pfizer, Tox Navigator includes toxicity data from regulatory documents and scientific articles.

Supporting the 3Rs and patient safety assessment, the Tox Navigator helps you:

  • Convert animal doses to human equivalent doses

  • Leverage existing data to reduce number of animal studies and design more efficient studies

  • Investigate adverse drug reactions across different species

  • Integrate in silico models and other non-animal testing methods

  • Optimize research efforts by focusing on candidates with favorable safety profiles

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Advance your research with Elsevierโ€™s PharmaPendium and a portfolio of solutions for pharmaceutical R&D.

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DDI risk calculator picto

FDA ๋ฐ EMA ๋ฌธ์„œ

๋‹ค๋ฅธ ์–ด๋–ค ๋„๊ตฌ์™€๋„ ๋น„๊ตํ•  ์ˆ˜ ์—†๋Š” ์™„์ „ํ•œ FDA ๋ฐ EMA ์Šน์ธ ํŒจํ‚ค์ง€์™€ ์ค‘์š”ํ•œ FDA ์ž๋ฌธ ์œ„์›ํšŒ ํšŒ์˜ ๋ฌธ์„œ๋กœ PharmaPendium์˜ ๊ฐ•๋ ฅํ•œ ๊ธฐ๋Šฅ์„ ํ™œ์šฉํ•˜์‹ญ์‹œ์˜ค.
Efficacy data picto

Enhanced visualization

Seamlessly move from table view to interactive charts, graphs and visual aids to easily interrogate and interpret data.
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Predictive tools

Predict harmful DDIs using the DDI Risk Calculator and the risk of off-target adverse events using the Safety Margin Tool.
Cultivate curiosity picto

๋น„๊ตํ•  ์ˆ˜ ์—†๋Š” ๊ฒ€์ƒ‰ ๊ธฐ๋Šฅ

์ •๊ทœํ™”๋œ ๋ฐ์ดํ„ฐ๋ฅผ ์‚ฌ์šฉํ•˜์—ฌ ๋ถ€์ž‘์šฉ(MedDRA), ํ‘œ์ , ์ ์‘์ฆ, ์•ฝ๋ฌผ ๋ฐ ์ข…์ ๋ณ„๋กœ ์ •๋ณด๋ฅผ ์ฐพ์Šต๋‹ˆ๋‹ค. ๊ฒฐ๊ณผ ํŽ˜์ด์ง€๋Š” ์ „์ž„์ƒ๊ณผ ์ž„์ƒ ๊ตฌ๋ถ„์„ ์—ฐ๊ฒฐํ•ฉ๋‹ˆ๋‹ค.
Reference picto

FAERS์˜ ์‹ค์ œ ์ฆ๊ฑฐ

FAERS(FDA ๋ถ€์ž‘์šฉ ๋ณด๊ณ  ์‹œ์Šคํ…œ)์—์„œ 1,900๋งŒ ๊ฐœ ์ด์ƒ์˜ ๋ณด๊ณ ์„œ๋ฅผ ๊ฒ€์ƒ‰ํ•˜์—ฌ ์‹ค์ œ ์ฆ๊ฑฐ ๋ฐ ์‹œํŒ ํ›„ ์•ฝ๋ฌผ ์•ˆ์ „์„ฑ์—์„œ ๋ถ€์ž‘์šฉ์„ ์ฐพ์Šต๋‹ˆ๋‹ค.
Data management picto

๊ณ ํ’ˆ์งˆ ๋ฐ์ดํ„ฐ ์„ธํŠธ

PharmaPendium์˜ ๊ณ ํ’ˆ์งˆ ๋ฐ์ดํ„ฐ ์„ธํŠธ๋Š” ํ”Œ๋žซํผ ์™ธ๋ถ€์—์„œ ์‚ฌ์šฉํ•  ์ˆ˜ ์žˆ์Šต๋‹ˆ๋‹ค. ๋ณด๋‹ค ์ •ํ™•ํ•œ ๊ฒ€์ƒ‰ ๋ฐ ์˜ˆ์ธก์„ ์œ„ํ•ด ์›Œํฌํ”Œ๋กœ์™€ ๋ชจ๋ธ์— ๋ฐ์ดํ„ฐ๋ฅผ ํฌํ•จํ•˜์„ธ์š”.

"... PharmaPendium excels in retrieving specific toxicity observations across approval documents categorized by drug and species."

Guy Bouvier

GB

Guy Bouvier, PhD, ERT

Groupe Pierre Fabre์˜ Director, Toxicology & Product Safety

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