Data management

99 Results

Using SDTM, ADaM, and SEND

Formedix | 09-Nov-2022 | Technical / White Paper

This article gives an overview of SDTM, ADaM, SEND and ARM, and discusses how these CDISC standards fit in with the wider clinical trial process, and how...

How to design an effective CRF

Formedix | 10-Oct-2022 | Technical / White Paper

CRFs and eCRFs are used for gathering patient data during clinical trials. They play a crucial role in helping to assess the safety and efficacy of clinical...

Automating clinical trials: Why it's essential

Formedix | 05-Sep-2022 | Technical / White Paper

Automation is used to improve the accuracy of results in the clinical trial process from study setup through to submission.

ODM and CDASH in CRF design

Formedix | 15-Aug-2022 | Technical / White Paper

The lesser-known Operational Data Model (ODM) standard is often overlooked as it's not required by any regulators. So, why should you be interested...

Standardizing data with NCI controlled terminology

Formedix | 18-Jul-2022 | Technical / White Paper

The use of consistent terminology within and between studies is critical to enabling an efficient trial process. CDISC standards such as CDASH, SDTM, SEND...

How clinical trial software can optimize trials

Formedix | 20-Jun-2022 | Technical / White Paper

This article explains the different types of clinical trial software available, and how it can be used to optimize the end to end clinical trials design...

Governing and Maintaining Clinical Data Standards

Veeva | 10-May-2022 | Technical / White Paper

Investing in data standards plays a huge role in improving the quality of clinical studies. But often, people don’t use the standards correctly, there...

What the Best Clinical Study Build Pros Do

Formedix | 09-May-2022 | Technical / White Paper

Getting your clinical study designed and built ready for data collection takes A LOT of work and expertise… you've got to do all your CRF designs;...

What should a clinical metadata repository do?

Formedix | 18-Apr-2022 | Technical / White Paper

Choosing a clinical metadata repository (MDR) software can be a tough task as the capabilities and features of your chosen MDR could make or break your...

BMS Adopts a New Clinical Data Architecture

eClinical Solutions | 31-Mar-2022 | Case Study

In this Case Study, you will learn how Bristol Myers Squibb optimized their data review processes to streamline and improve access to their data. By implementing...

How The Supply Chain Has Been Impacted By COVID-19

Catalent | 31-Mar-2022 | Insight Guide

The pharmaceutical industry had to adapt quickly to the pandemic if it was to continue to supply important medicines, while also racing to develop vaccines...

How Can You Avoid Delays in Your Trial? - Strategies for Comparator Sourcing

Catalent | 29-Mar-2022 | Insight Guide

An optimized approach to comparator sourcing can improve inventory management and supply chain performance. This article summarizes key factors to comparator...

Achieve Clean Data Sets Faster

eClinical Solutions | 28-Mar-2022 | Case Study

In this case study, you will learn how Karyopharm Therapeutics simplified their data flow and reduced manual work across a diverse pipeline of clinical...

The ryze-elluminate integration in clinical trials

Formedix | 28-Mar-2022 | Technical / White Paper

The integration between Formedix's ryze CMDR and eClinical's elluminate CDR maximizes automation across the end-to-end clinical trial lifecycle....

For eCOA Success, Look For The Four S's

Signant Health | 21-Mar-2022 | Technical / White Paper

For an effective eCOA platform that can meet any protocol requirements, study teams need more than just an app. Download this perspective paper to learn...

Opportunities to Accelerate Decentralized Trials

eClinical Solutions | 21-Mar-2022 | Technical / White Paper

Take a deeper look into the current state of data sources, organization, and analytics in this white paper. You will learn about their impact and the opportunities...

The Clinical Development Digitization Guide

eClinical Solutions | 07-Mar-2022 | Technical / White Paper

Take a deeper look into the key components of preparing for the digitization of today's clinical trials in this white paper. You will learn the necessary...

What’s Next for mRNA?

Catalent Pharma Solutions | 27-Jan-2022 | Insight Guide

Now that the pharma industry and regulators have significant data on safety and efficacy of mRNA vaccines, many companies are looking beyond infectious...

SmartSignals Study Oversight

Signant Health | 24-Jan-2022 | Product Brochure

Today, sponsors and study teams often struggle to support the growing variety and volume of clinical data. The right technology thought will help your...

The APAC Advantages

Catalent Pharma Solutions | 18-Jan-2022 | Insight Guide

Over recent years, the Asia-Pacific (APAC) region has become an emerging market for pharmaceutical and biotech innovation, including clinical studies.

How a Clinical MDR Helps with Data Quality

Formedix | 17-Jan-2022 | Technical / White Paper

This article covers the many ways a clinical metadata repository helps with data quality in the clinical trial process, and how it ultimately helps to...

The Case for a Clinical Data Strategy

eClinical Solutions | 12-Jan-2022 | Technical / White Paper

Being data-driven is top-of-mind for many life sciences companies, but actually turning that idea into action is easier said than done. To effectively...

Optimizing Processes for Modern Digital Trials

eClinical Solutions | 12-Jan-2022 | Case Study

Modern digital trials have sparked a new need within life sciences organizations for optimized and scalable clinical data processes & strategies. This...

How Can a Supply Chain Dashboard Yield Greater Clinical Trial Insights, Cost Control, and Efficiency?

Ancillare | 10-Jan-2022 | Technical / White Paper

With 1 in 10 Sponsors identifying a lack of technology integration as their biggest pain point, Deighton Liverpool, Ancillare’s Chief Information Officer...

Efficient Clinical Supply Management & Forecasting

Catalent Pharma Solutions | 30-Nov-2021 | Insight Guide

How can clinical supply management benefit your trials? Download this eBook to explore how you can drive excellence within the forecasting process, as...

Proof of Concept: Virtual Site Selection Visit (SSV)

Signant Health | 22-Nov-2021 | Case Study

The recent pandemic inspired Bayer to a proof-of-concept (POC) study that identified a viable solution for replacing in-person site selection visits. The...

COVID-19 Vaccine Studies Succeed with Support from Signant Health

Signant Health | 25-Oct-2021 | Case Study

Signant helped a leading sponsor meet accelerated timelines while generating high-quality COVID-19 vaccine safety and efficacy endpoint data.

Paper vs ePRO Data Collection Methods

Signant Health | 19-Oct-2021 | Technical / White Paper

Are you curious why more Sponsors choose digital data collection methods over the traditional pen and paper? Read this recent white paper to discover the...

GLP Tissue Cross Reactivity Testing

Precision for Medicine | 11-Oct-2021 | Product Brochure

Precision for Medicine's unique combination of research services and tissue procurement capabilities form the pillars of our GLP Tissue Cross Reactivity...

Automating clinical trials for success

Formedix | 06-Oct-2021 | Technical / White Paper

This article gives gives a brief overview of why automation is absolutely essential for clinical trial success.

Next Generation Immune Monitoring: Epiontis ID

Precision for Medicine | 04-Oct-2021 | Data Sheet

Rapid and consistent results, flexibility in sample type, and minimal sample processing to support global clinical studies

New Clinical MDR & Automation Platform by Formedix

Formedix | 16-Aug-2021 | Data Sheet

Formedix, a leading provider of clinical trial software solutions, announces the launch of ryze, an innovative all-in-one cloud-based clinical metadata...

Top Pharmaceutical Company Drives Strategic Resource Management and Portfolio Planning

PerkinElmer | 04-Aug-2021 | Case Study

With a portfolio of clinical studies that fluctuates year over year depending on the portfolio, resource and cost constraints are a constant issue. Questions...

Advanced Analytics Driving Interactive Data Exploration in Study Teams

PerkinElmer | 15-Jul-2021 | Technical / White Paper

At Novartis, TIBCO Spotfire® enterprise analytics is a key tool for interactive graphical data analysis for preclinical and clinical studies. Using interactive...

Empowering Clinical Trial Sponsors with Analytics

PerkinElmer | 14-Jul-2021 | Technical / White Paper

Is your Clinical Data Review creating problems or solving them? Take Control of Your Data. PerkinElmer Informatics Clinical Solutions, powered by Tibco...

Achieving Greater Efficiencies with Advanced Data Capturing and Monitoring

PerkinElmer | 01-Jul-2021 | Data Sheet

With larger, more complex clinical trials, along with more stringent regulatory requirements and oversight, integrating and managing vast amounts of data...

Overcoming Challenges of Clinical Data Review

PerkinElmer | 10-Jun-2021 | Technical / White Paper

Clinical data review is intrinsic to clinical development, assuring patient safety, determining drug efficacy, and assessing data quality. It involves...

The Key to a Faster, More Flexible Clinical Trial Process

PerkinElmer | 10-Jun-2021 | Technical / White Paper

Clinical development teams are under enormous pressure to navigate the lengthy and challenging clinical trial process, often needing to alchemize these...

Advancing Opportunities for Success in Central Nervous System Clinical Trials

Signant Health | 31-May-2021 | Insight Guide

The clinical development process for novel therapies that treat central nervous system (CNS) diseases is scientifically and medically complex, as demonstrated...

TIBCO Spotfire® as Essential Tool at Major Global Pharmaceutical Company

PerkinElmer | 03-May-2021 | Case Study

A decade after its initial implementation for a small group of R&D users, PerkinElmer’s TIBCO Spotfire® visual analytics and discovery platform is...

Transforming Clinical Development

PerkinElmer | 01-May-2021 | Technical / White Paper

The estimated cost of bringing a drug to market in the U.S. according to JAMA is $1 billion.1 The extreme cost of clinical trials urge biopharmaceutical,...

What are the building blocks of DCTs?

Medable | 26-Apr-2021 | Technical / White Paper

How to create a seamless experience across eConsent, eCOA and more.

Over the past year, tremendous progress was made toward digitizing and...

Virtual Trials: Trust in Experience, Trust in Lunexis™

Clinical Ink | 24-Mar-2021 | Data Sheet

From Infectious Disease to BYOD, We Set the Bar for Virtual Trials

Introduction to eLAS®

Clinical Ink | 08-Mar-2021 | Product Brochure

Clinical Ink has developed a unique offering — the electronic Lupus Assessment Suite (eLAS®) to address fundamental challenges impacting systemic lupus...

Deploy Configurable, Mixed-Modality ePRO Solutions, Fast

Clinical Ink | 01-Mar-2021 | Data Sheet

Real-Time, Integrated Data Capture With Unprecedented Freedom of Choice

A Winning End-to-End Solution for Oncology Studies

Clinical Ink | 22-Feb-2021 | Technical / White Paper

Oncology clinical trials present a unique set of challenges for patients, study sites, and study sponsors. Using electronic patient reported outcomes (ePRO)...

Global Clinical Trial Lab Services

Q² Solutions | 01-Apr-2020 | Product Presentation

As a leading global lab services partner, we provide operational excellence, scientific leadership and innovation through technology. We offer end-to-end...

Outsourcing Analytical Testing for Biologics - A CRO's Perspective

Frontage Laboratories | 01-Dec-2019 | Technical / White Paper

Biologics are complex large molecules derived from living organisms or manufactured from cells, and they have inherent structural heterogeneity. Indeed,...

Validating The Simoa Technology

Frontage Laboratories | 01-Oct-2019 | Technical / White Paper

Frontage is the first and only laboratory to validate Quanterix’ Simoa HD1 Analyzer for performing immunoassays. Most of the advanced instruments used...

How to Avoid Surprises in Small-Molecule Drug Development Programs

Frontage Laboratories | 01-Oct-2019 | Technical / White Paper

Over the years, the pharmaceutical industry has made steady progress in improving the safety of drugs in development. Consequently, in 2015, only 14 percent...

Outsourcing-Pharma

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