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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...

The Effect of PVP Viscosity on the Binding Performance in Naproxen Tablets

Content provided by JRS PHARMA | 01-Aug-2022 | Clinical Study

This study aimed to compare the performance of VIVAPHARM® PVP K25, VIVAPHARM® PVP K30, and VIVAPHARM® PVP K90 respectively as wet-granulation binders in...

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

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

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...

Is Your Ancillary Supply Chain Supporting Trial Success?

Content provided by Ancillare | 06-Jul-2022 | White Paper

As the effects of the pandemic reverberate through global supply chains, Sponsors still face many hurdles in sourcing and managing ancillary supplies for...

Formulation Effects on Tablet Surface Properties and Film Coating Adhesion

Content provided by JRS PHARMA | 01-Jul-2022 | White Paper

The aim of this study was to investigate the influence of different commonly applied lubricants and disintegrants on tablet surface and film coating adhesion....

Pediatric Formulations: Identifying & Addressing Children’s Needs

Content provided by Piramal Pharma Solutions | 30-Jun-2022 | White Paper

Developing formulations for pediatric patients poses unique challenges. The specific needs of children, which vary by age, mean the task goes beyond scaling...

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

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

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

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

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

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;...

Home Health in Clinical Trials — A Better Way to Meet Patients’ Needs

Content provided by Firma Clinical Research | 13-Apr-2022 | Infographic

Meeting patient needs today is complicated. But there is one thing that can minimize their burden, improve retention, and maximize protocol compliance....

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

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

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...

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

Content provided by 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...

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

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

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

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...

Psychedelics and Entactogens: Challenges Associated with Schedule I Therapeutic Development

Content provided by Altasciences | 18-Mar-2022 | White Paper

Under the Controlled Substances Act (CSA) in the United States, drugs that have the potential to be abused are scheduled into one of five Classes or Schedules...

Discover the endless opportunities our Softgel Capsule can offer to your brand.

Content provided by Sofgen Pharmaceuticals | 17-Mar-2022 | Product Catalog

The softgel capsule has been on the market since the 19th century evolving to the present day. Because of this, consumers feel familiar with the technology...

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...

Procaps Group Acquires 1st U.S.-Based Softgel Production Facility under the name Sofgen Pharmaceuticals, expanding its iCDMO Business Unit.

Content provided by Sofgen Pharmaceuticals | 14-Mar-2022 | Press Release

As a leading pharmaceutical group, Procaps is focused on the expansion of its iCDMO business, offering integrated, end-to-end solutions in innovative softgel...

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

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

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

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)...

Funtrition by Procaps expands its gummy offerings with new Gummy manufacturing facility in the US

Content provided by Sofgen Pharmaceuticals | 14-Feb-2022 | Press Release

New Funtrition Gummy Manufacturing Facility in Florida Slated to be Fully Operational by Q1 2023, to Support Increased U.S. and global Demand of Advanced...

Spray Dried Powders for High Dose Drug Delivery

Content provided by Catalent | 01-Feb-2022 | Product Presentation

This Catalent webinar will explore how spray dried particles provide an attractive, carrier-free option for highly dispersed delivery of API to deep lung...

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

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

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.

CellCarta - Mapping Precision Medicine

Content provided by CellCarta | 17-Jan-2022 | Product Presentation

At CellCarta, we’re dedicated to working with our partners to further the limitless potential of precision medicine. Our broad technology offering is designed...

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

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

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...

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

Content provided by Ancillare | 10-Jan-2022 | 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...

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...

The Future of Innovation In Pharmaceutical Delivery Systems

Content provided by Sofgen Pharmaceuticals | 06-Dec-2021 | Product Presentation

More than 4 decades of expertise in innovative technologies and value-added pharmaceutical solutions. Procaps Group's purpose is to spread its legacy...

A Culture of Innovation as a Differentiation

Content provided by Sofgen Pharmaceuticals | 06-Dec-2021 | Product Presentation

We create safe, effective and differentiated pharmaceutical solutions and this has been our goal since day 1. The main driver of our growth is innovation...

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)

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

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...

INDENA’S CUSTOM DEVELOPMENT AND MANUFACTURING SERVICES FOR APIS AND HPAPIS

Content provided by Indena | 08-Nov-2021 | White Paper

Indena’s Custom Development & Manufacturing Organization services oﬀers a full range of manufacturing capabilities for pharmaceutical ingredients....

COVID-19 Vaccine Studies Succeed with Support from Signant Health

Content provided by 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.

APAC Region Distribution Considerations for Clinical Trial Supplies

Content provided by Catalent | 19-Oct-2021 | Insight Guide

The Asia-Pacific (APAC) region has been a steadily growing area for sponsors to conduct clinical studies. Maintaining continuity of trial supply across...

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