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Case Study: SmartSignals eConsent

Case Study: SmartSignals eConsent

Content provided by Signant Health | 15-Feb-2022 | Case Study

Signant’s eConsent solution helped a sponsor manage the consenting process complexities in their pediatric attention deficit hyperactivity disorder (ADHD)...

What’s Next for mRNA?

What’s Next for mRNA?

Content provided by Catalent | 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

SmartSignals Study Oversight

Content provided by 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

The APAC Advantages

Content provided by Catalent | 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.

Planning Your Preclinical Assessment

Planning Your Preclinical Assessment

Content provided by Altasciences | 17-Jan-2022 | White Paper

There are many challenges associated with early drug discovery and development. Advancing your best candidate for regulatory submissions requires a careful...

The Case for a Clinical Data Strategy

The Case for a Clinical Data Strategy

Content provided by eClinical Solutions | 12-Jan-2022 | 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

Optimizing Processes for Modern Digital Trials

Content provided by 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...

Maximizing Drug Formulation for First-In-Human Trials

Maximizing Drug Formulation for First-In-Human Trials

Content provided by Altasciences | 13-Dec-2021 | Case Study

The manufacture of a drug product for clinical trials is of critical importance. The formulation, manufacturing, and assessment of a drug candidate during...

Efficient Clinical Supply Management & Forecasting

Efficient Clinical Supply Management & Forecasting

Content provided by Catalent | 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)

Proof of Concept: Virtual Site Selection Visit (SSV)

Content provided by 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...

Flexibility and capability in pre-filled syringes

Flexibility and capability in pre-filled syringes

Content provided by Curia | 15-Nov-2021 | White Paper

Pre-filled syringes have risen in popularity in recent years but the pandemic’s impact on drug development, manufacturing and patient care has created...

Paper vs ePRO Data Collection Methods

Paper vs ePRO Data Collection Methods

Content provided by Signant Health | 19-Oct-2021 | 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...

LACTIUM®: dairy bioactive to soothe your pet

LACTIUM®: dairy bioactive to soothe your pet

Content provided by Ingredia | 12-Oct-2021 | Infographic

Lactium® gives you the chance to better meet your pet’s needs for a more harmonious life together. Lactium® acts on the brain and has no side-effects,...

GLP Tissue Cross Reactivity Testing

GLP Tissue Cross Reactivity Testing

Content provided by 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

Automating clinical trials for success

Content provided by Formedix | 06-Oct-2021 | 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

Next Generation Immune Monitoring: Epiontis ID

Content provided by Precision for Medicine | 04-Oct-2021 | Infographic

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

A Better Approach, for Better Pain Trials

A Better Approach, for Better Pain Trials

Content provided by Signant Health | 27-Sep-2021 | White Paper

Pain studies face unique challenges. For one, pain severity can only be truly assessed by the patients themselves. The controlled substances that are often...

Facilities: Lexington, KY USA

Facilities: Lexington, KY USA

Content provided by Piramal Pharma Solutions | 23-Aug-2021 | Insight Guide

The Piramal Pharma Solutions facility in Lexington, KY USA is a fully integrated site which offers analytical, formulation development, and manufacturing...

Facilities: Sellersville, PA USA

Facilities: Sellersville, PA USA

Content provided by Piramal Pharma Solutions | 23-Aug-2021 | Insight Guide

The Piramal Pharma Solutions facility in Sellersville, PA USA is a fully integrated site that offers product and process development, clinical supply and...

New Clinical MDR & Automation Platform by Formedix

New Clinical MDR & Automation Platform by Formedix

Content provided by Formedix | 16-Aug-2021 | Infographic

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

Facilities: Riverview, MI USA

Facilities: Riverview, MI USA

Content provided by Piramal Pharma Solutions | 26-Jul-2021 | Insight Guide

The Piramal Pharma Solutions facility in Riverview, MI, USA can support your Drug Substance (API) needs. The site has extensive experience in safely delivering...

Facilities: Morpeth, UK

Facilities: Morpeth, UK

Content provided by Piramal Pharma Solutions | 26-Jul-2021 | Insight Guide

The Piramal Pharma Solutions facility in Morpeth, UK offers Active Pharmaceutical Ingredients (APIs) and oral solid drug product development, clinical...

Adapting supply chains to new ways of working

Adapting supply chains to new ways of working

Content provided by World Courier | 15-Jul-2021 | White Paper

COVID-19 has changed the way we operate. We have adapted our supply chain solutions to meet our clients’ requirements while following World Courier standard...

Empowering Clinical Trial Sponsors with Analytics

Empowering Clinical Trial Sponsors with Analytics

Content provided by PerkinElmer | 14-Jul-2021 | White Paper

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

Facilities: Grangemouth, UK

Facilities: Grangemouth, UK

Content provided by Piramal Pharma Solutions | 28-Jun-2021 | Insight Guide

The Piramal Pharma Solutions site in Grangemouth, UK offers development, clinical & commercial scale manufacture of bio-conjugates including Antibody...

Facilities: Aurora, Canada

Facilities: Aurora, Canada

Content provided by Piramal Pharma Solutions | 28-Jun-2021 | Insight Guide

The Piramal Pharma Solutions facility in Aurora Canada offers development, clinical and commercial GMP manufacturing of Active Pharmaceutical Ingredients...

Overcoming Challenges of Clinical Data Review

Overcoming Challenges of Clinical Data Review

Content provided by PerkinElmer | 10-Jun-2021 | White Paper

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

Integrated Solutions for Accelerated Time to Market

Integrated Solutions for Accelerated Time to Market

Content provided by Piramal Pharma Solutions | 08-Jun-2021 | White Paper

Facing capacity constraints? Lock in your program now! With 14 sites around the world providing diverse services ranging from discovery to drug substance...

Transforming Clinical Development

Transforming Clinical Development

Content provided by PerkinElmer | 01-Jun-2021 | 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?

What are the building blocks of DCTs?

Content provided by Medable | 26-Apr-2021 | White Paper

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

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

Pharma Manufacturing: Attaining the Right Global Mix

Pharma Manufacturing: Attaining the Right Global Mix

Content provided by Curia | 13-Apr-2021 | White Paper

The COVID-19 pandemic has brought the global interdependency of pharmaceutical supply chains into sharp focus, exposing weak links & re-igniting discussions...

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