White Paper Archives

Guide White Paper

A Practical Guide to Creating Effective Budget Impact Models

BaseCase empowers market access, medical, and sales teams to effectively engage decision-makers by translating complex…

CertaraJuly 1, 2025

White Paper

Everything you need to know about ILAP 2.0

This white paper share’s key insights on the relaunch of MHRA’s Innovative Licensing and Access…

CertaraMay 19, 2025

White Paper

Rare Oncology Product Launch Playbook: Universal Strategies for Success in the U.S. and Europe

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CertaraFebruary 28, 2025

White Paper

The Benefits of Real-Time Nonclinical Safety Data Analysis

Learn how SEND Explorer software helps nonclinical drug developers streamline performing real-time toxicology assessments of…

CertaraJanuary 27, 2025

White Paper

Clinical Metadata Standardization: Evaluating the Importance of a Metadata Repository in Clinical Trials

Whether you’re considering a metadata repository or want to learn about clinical metadata standardization, our…

CertaraNovember 22, 2024

White Paper

Streamline Regulatory Writing with AI-Powered Solutions

Learn how tailored AI solutions streamline regulatory writing, boosting efficiency, accuracy, & compliance.

CertaraNovember 14, 2024

White Paper

Assessing Transporter-Mediated DDIs

Discover strategies for evaluating transporter-mediated drug-drug interactions (DDIs) and their impact on drug safety, efficacy,…

CertaraOctober 21, 2024

White Paper

Clinical Trial Data Sharing Under EMA Policy 0070

CertaraOctober 9, 2024

White Paper

Evaluating the IRA’s Impact on Medicare Part B Biosimilar Reimbursement

White paper exploring the IRA’s small but measurable impact in several key areas

CertaraAugust 13, 2024

White Paper

DSURs, RMPs, and PSURs – The Harmonization of Pharmacovigilance Documents

CertaraJuly 30, 2024

White Paper

A Practical Guide to Creating Effective Budget Impact Models

Everything you need to know about ILAP 2.0

Rare Oncology Product Launch Playbook: Universal Strategies for Success in the U.S. and Europe

The Benefits of Real-Time Nonclinical Safety Data Analysis

Clinical Metadata Standardization: Evaluating the Importance of a Metadata Repository in Clinical Trials

Streamline Regulatory Writing with AI-Powered Solutions

Assessing Transporter-Mediated DDIs

Clinical Trial Data Sharing Under EMA Policy 0070

Evaluating the IRA’s Impact on Medicare Part B Biosimilar Reimbursement

DSURs, RMPs, and PSURs – The Harmonization of Pharmacovigilance Documents

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