주요 콘텐츠로 건너뛰기

귀하의 브라우저가 완벽하게 지원되지 않습니다. 옵션이 있는 경우 최신 버전으로 업그레이드하거나 Mozilla Firefox, Microsoft Edge, Google Chrome 또는 Safari 14 이상을 사용하세요. 가능하지 않거나 지원이 필요한 경우 피드백을 보내주세요.

이 새로운 경험에 대한 귀하의 의견에 감사드립니다.의견을 말씀해 주세요

Elsevier
엘스비어와 함께 출판

PharmaPendium은 더 나은 약물 결과를 위해 약물 안전성 및 효능 결정을 지원합니다.

자신 있게 발견, 혁신 및 개발하려면 고품질 데이터가 필요합니다. PharmaPendium은 비교할 수 없는 규제 및 약물 데이터를 전체 텍스트 검색 및 예측 도구와 결합합니다. PharmaPendium으로 동물 실험을 줄이고 약물을 더 빠르게 출시하십시오.

Women in white lab coats looking at computer screen

FDA 및 세계 최고의 제약 회사에서 사용

Get critical insights to predict the success or failure of drug candidates as early as possible

Video overview of PharmaPendium

Watch now

|

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

  • Predict the risk of off-target adverse drug reactions (safety margin)

  • 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)

Watch an introductory video

Make informed decisions to increase the success of regulatory submissions

Female professional talking to colleague

Minimize regulatory cycling and avoid failing approval with PharmaPendium.

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

  • Explore previous regulatory submissions and learn from precedents to predict agencies’ requirements

  • Benchmark against approved and withdrawn drugs with the same mechanism of action as your drug candidates

  • 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

Connected, configurable solutions to innovate in R&D

Advance your research with Elsevier’s PharmaPendium and a portfolio of solutions for pharmaceutical R&D.

Innovate with confidence, supported by:

  • Trusted quality information from regulatory data to peer-reviewed scientific literature

  • Innovative technology that powers data transformation and analytical and predictive tools

  • Domain and data science expertise to solve complex problems with data solutions for R&D

Information integrity is essential to your progress. Discover trusted data and tools that deliver critical insights.

Let's shape progress together.

Find precise data to advance your drug portfolio

DDI risk calculator picto

FDA 및 EMA 문서

다른 어떤 도구와도 비교할 수 없는 완전한 FDA 및 EMA 승인 패키지와 중요한 FDA 자문 위원회 회의 문서로 PharmaPendium의 강력한 기능을 활용하십시오.
Efficacy data picto

Enhanced visualization

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

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

비교할 수 없는 검색 기능

정규화된 데이터를 사용하여 부작용(MedDRA), 표적, 적응증, 약물 및 종점별로 정보를 찾습니다. 결과 페이지는 전임상과 임상 구분을 연결합니다.
Reference picto

FAERS의 실제 증거

FAERS(FDA 부작용 보고 시스템)에서 1,900만 개 이상의 보고서를 검색하여 실제 증거 및 시판 후 약물 안전성에서 부작용을 찾습니다.
Data management picto

고품질 데이터 세트

PharmaPendium의 고품질 데이터 세트는 플랫폼 외부에서 사용할 수 있습니다. 보다 정확한 검색 및 예측을 위해 워크플로와 모델에 데이터를 포함하세요.

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

Guy Bouvier

GB

Guy Bouvier, PhD, ERT

Groupe Pierre Fabre의 Director, Toxicology & Product Safety

Frequently asked questions

PharmaPendium Support Center

Get user-friendly tools to help you analyze drug safety, deliverability and efficacy data

Business people in meeting