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How a Clinical MDR Helps with Data Quality

How a Clinical MDR Helps with Data Quality

Content provided by Formedix | 16-Jan-2023 | 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...

Understanding the hidden value of quality

Understanding the hidden value of quality

Content provided by Thermo Fisher Scientific – Production Chemicals and Services | 16-Jan-2023 | White Paper

The raw material supply is too vital to leave to chance, and quality-related supply chain activities are cornerstones to your success.

Optimizing Adherence in DCTs

Optimizing Adherence in DCTs

Content provided by PPD - Decentralized Clinical Trials | 12-Jan-2023 | White Paper

Prioritizing greater patient-centricity and creating an opportunity to reach unprecedented patient groups, decentralized and hybrid clinical trials are...

PPD is Supporting Complex EU DCTs

PPD is Supporting Complex EU DCTs

Content provided by PPD - Decentralized Clinical Trials | 05-Jan-2023 | White Paper

PPD supports European DCTs and clinical trial sponsors with a holistic and comprehensive approach

What should a clinical metadata repository do?

What should a clinical metadata repository do?

Content provided by Formedix | 14-Dec-2022 | 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...

Helping Trial Sites Overcome Prevailing DCT Challenges

Helping Trial Sites Overcome Prevailing DCT Challenges

Content provided by PPD - Decentralized Clinical Trials | 13-Dec-2022 | White Paper

As a CRO, PPD (part of Thermo Fisher) can help guide the future of clinical research. Its depth of experience with decentralized clinical trials (DCTs)...

Using SDTM, ADaM, and SEND

Using SDTM, ADaM, and SEND

Content provided by Formedix | 09-Nov-2022 | 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...

INDENA ALWAYS AT THE FOREFRONT FOR CDMO SERVICES

INDENA ALWAYS AT THE FOREFRONT FOR CDMO SERVICES

Content provided by Indena | 25-Oct-2022 | White Paper

Indena is well known in the space of naturally derived molecules, with a know-how developed over its one hundred year history. At the same time, the company...

How to design an effective CRF

How to design an effective CRF

Content provided by Formedix | 10-Oct-2022 | 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...

The Complexities of Ophthalmic Drug Development

The Complexities of Ophthalmic Drug Development

Content provided by Altasciences | 04-Oct-2022 | White Paper

Ophthalmic drug development comes with a unique set of challenges that can be mitigated by working with an end-to-end solution provider with regulatory...

Because When It's On the Line... Capability Matters.

Because When It's On the Line... Capability Matters.

Content provided by Baxter BioPharma Solutions | 01-Oct-2022 | Product Brochure

Baxter’s BioPharma Solutions business supports leading pharmaceutical companies in meeting their commercialization objectives by providing scientific expertise,...

dPCR Case Study

dPCR Case Study

Content provided by CellCarta | 08-Aug-2022 | Case Study

Streamline your adoptive cell therapy program with digital PCR. Our team has a unique expertise in digital and quantitative PCR to support you in ensuring...

Planning Your First-In-Human Trial

Planning Your First-In-Human Trial

Content provided by Altasciences | 15-Jul-2022 | White Paper

A first-in-human (FIH) clinical trial is a significant milestone in the development of a potential new drug. A successfully conducted FIH trial provides...

Seasonal Vaccine Manufacturing

Seasonal Vaccine Manufacturing

Content provided by Baxter BioPharma Solutions | 13-Jul-2022 | White Paper

The production of seasonal vaccines, such as those for influenza, presents unique challenges to manufacturers due to the necessary time constraints resulting...

Consideration and Options for Prefilled Syringes

Consideration and Options for Prefilled Syringes

Content provided by Baxter BioPharma Solutions | 13-Jul-2022 | White Paper

Convenience, product differentiation, and less waste are great reasons for developing a product in a prefilled syringe. Baxter’s whitepaper describes the...

Multiple Sclerosis Analytical Report

Multiple Sclerosis Analytical Report

Content provided by PatSnap | 15-Jun-2022 | White Paper

More than 2.3 million people are living with MS worldwide. Although there is no cure, new research and innovative treatments are continuously emerging....

Implementing Patient Co-Creation in Clinical Trials

Implementing Patient Co-Creation in Clinical Trials

Content provided by THREAD | 14-Jun-2022 | Insight Guide

Patient co-creation in clinical research means a shift from thinking about the patient to thinking with the patient. This means that patients are giving...

Flexible Filling Solution for CMOs

Flexible Filling Solution for CMOs

Content provided by Single Use Support GmBH | 18-May-2022 | Insight Guide

Achieving flexibility requires modularity of technologies.

CMOs and CDMOs aspire to be flexible for multiple applications. Efficient automated...

Strategic Approach to Immunogenicity Assessment

Strategic Approach to Immunogenicity Assessment

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

In this issue of The Altascientist we provide a detailed overview on the different goals and challenges that are presented by the validation of immunogenicity...

Governing and Maintaining Clinical Data Standards

Governing and Maintaining Clinical Data Standards

Content provided by Veeva | 10-May-2022 | 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

What the Best Clinical Study Build Pros Do

Content provided by Formedix | 09-May-2022 | 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;...

Nanomilling for Better Solubility and Bioavailability

Nanomilling for Better Solubility and Bioavailability

Content provided by Altasciences | 07-Apr-2022 | White Paper

40% of marketed drugs and 90% of active pharmaceutical ingredients (APIs) are poorly water-soluble. Nanomilling is a proven technique that can overcome...

BMS Adopts a New Clinical Data Architecture

BMS Adopts a New Clinical Data Architecture

Content provided by 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

How The Supply Chain Has Been Impacted By COVID-19

Content provided by 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...

The ryze-elluminate integration in clinical trials

The ryze-elluminate integration in clinical trials

Content provided by Formedix | 28-Mar-2022 | White Paper

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

Achieve Clean Data Sets Faster

Achieve Clean Data Sets Faster

Content provided by 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...

For eCOA Success, Look For The Four S's

For eCOA Success, Look For The Four S's

Content provided by Signant Health | 21-Mar-2022 | 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

Opportunities to Accelerate Decentralized Trials

Content provided by eClinical Solutions | 21-Mar-2022 | 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...

Eastern & Western Manufacturing Solutions

Eastern & Western Manufacturing Solutions

Content provided by Piramal Pharma Solutions | 15-Mar-2022 | White Paper

The best manufacturing site for a product can change throughout the life cycle. When bringing new drugs to market, biopharma companies may benefit from...

The Clinical Development Digitization Guide

The Clinical Development Digitization Guide

Content provided by eClinical Solutions | 07-Mar-2022 | 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...

How Formulation Development Affects Manufacturing

How Formulation Development Affects Manufacturing

Content provided by Catalent | 24-Feb-2022 | Insight Guide

Due to advances in technology and increased development of parenteral drugs, one of the fastest-growing choices for drug delivery in the pharmaceutical...

Clear Guidelines for IND/CTA

Clear Guidelines for IND/CTA

Content provided by Altasciences | 24-Feb-2022 | White Paper

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

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.

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