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Pharmapendium

Supporting your critical drug development decisions

PharmaPendium is a unique information management tool designed to answer all your drug development and pharmacological questions. It supports you with the critical decisions at every stage of your drug development process. It offers searchable FDA approval packages and EMA EPARs and brings together excerpted preclinical, clinical, and post-marketing safety data into a single longitudinal database. With crucial comparative data and access to regulatory precedents, the PharmaPendium database supports you in your clinical research and helps to improve drug development workflows and the approval process. PharmaPendium is the definitive source for your drug development information needs.
Pharmapendium about

 

Guide Your Research

Essential and relevant data from the best sources to support your decisions

Decisions in every stage of drug development need the best information resources. The PharmaPendium database contains the most essential and relevant regulatory documents, scientific literature and commercial information for drug research. Only PharmaPendium brings you such a wealth of cutting-edge and historical biological and pharmacological data, and the optional Pharmokinetics and Metabolizing Enzymes modules increase the power of your information searches in specific areas. Discover what other search engines miss, learn from past submission mistakes, find out how to present the most compelling regulatory cases, and gain and maintain your market position. Trust PharmaPendium to guide your research.

 

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Accelerate Drug Development

Powerful software that quickly and accurately retrieves drug data

Drug development is a highly dynamic field. PharmaPendium makes it easy to retrieve relevant and accurate data on preclinical and clinical drug efficacy, safety and pharmokinetics. The PharmaPendium database is meticulously indexed and hierarchically structured so you can quickly reach comparative data on candidates sharing any similarities. The optional Pharmokinetics and Metabolizing Enzymes modules follow the same optimized architecture. Speed up your drug development process with PharmaPendium.

 

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Discover PharmaPendium

Our brochure describes all of the features of PharmaPendium and gives details of how the optional modules integrate into your workflows.

Download the brochure (9 MB)

 

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See the Benefits

We have prepared a video to show how PharmaPendium can benefit you.

Watch the video

 

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Search Intelligently

Unique features that deliver superior results

Information management tools must be designed with the end user in mind. PharmaPendium is designed and curated for every stage of drug development research, with scores of searchable drug reviews and data, access to regulatory precedents, and databases carefully mapped by a team of experts. Key features include:

  • Text searching with synonym recognition
  • Structure searching, including structure similarity and substructure
  • Browsing by drug name, class and target information
  • Browsing by adverse effect and toxicity
  • Comparisons of adverse effects and species specificity across drugs and drug classes

Information management tools must be designed with the end user in mind. PharmaPendium is designed and curated for every stage of drug development research, with scores of searchable drug reviews and data, access to regulatory precedents, and databases carefully mapped by a team of experts. Key features include text searching with synonym recognition; structure searching with structure similarity and substructure options; browsing by drug name, class or target, or by adverse effect and toxicity; and cross-drug and -drug class comparisons of adverse effects and species specificity.

 

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Access Regulatory Documents

Optional module increases access to EMA, AERS and FDA documents

Access to FDA, EMA and AERS documentation is essential if your drug candidate is to gain approval and have competitive advantages in its class. PharmaPendium gives you access to regulatory information from preclinical and clinical trials and approval documents to give you that competitive edge and support you in preparing all-important applications to regulatory authorities. The optional Pharmacokinetics Module gives you unprecedented access to preclinical and clinical exposure data extracted from the entire history of FDA Approval Packages and EMA documents. Read more about the Pharmokinetics Module here.

 

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Reveal Drug-Drug Interactions

Optional module increases information on drug-metabolizing enzyme and transporter effects

Metabolizing Enzymes Module is a major resource for the modeling of adverse drug interactions resulting from the effects of drug-metabolizing enzymes and transporters. Enjoy the benefits of a unique content source that presents an unmatched level of data on CYP enzymes, Phase 2 enzymes, and dynamic pharmacokinetic parameters in context. Read more about the Metabolizing Enzymes Module here.

 

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Pharmapendium® and the Pharmapendium® trademark are owned and protected by Reed Elsevier Properties SA. All rights reserved.