Whitepapers

Download this whitepaper to get a better understanding of the evolving regulatory guidelines for cell and gene therapies, in order to bring them to market faster.

This article exposes how CFD simulations can help us to face challenging designs involving fluid mechanics and thermal phenomena accurate study.

In pharma delivery, size matters. So, too, do the intricacies of dosage format, active ingredient compatibility, and effective delivery to patients—whatever their needs or preferences may be. Yet standard dosage forms haven’t always provided companies the options, flexibility, or performance to bring all those puzzle pieces together during therapeutic development. We spoke with Nathan H. Dormer, PhD, Director of Drug Product Development at Adare Pharma Solutions, to learn how this new technology platform is expanding the frontiers of therapeutic delivery and improving patients’ experience in the process.

This whitepaper explores vaccine development during a pandemic, a response to complex challenges that traditional manufacturing methods won’t solve.

As the industry—and the world—faces unprecedented challenges, your choice of CDMO plays an increasingly important role in the success of your project. New formulations and underserved patient populations demand a level of expertise many development and manufacturing partners simply don’t have. Is your CDMO partner able to adapt to today’s ever-changing world? Giovanni Ortenzi, the leader of Adare Pharma’s global pharmaceutical development and technical services, was recently interviewed about how Adare is uniquely qualified to meet and overcome these new challenges. Adare’s unique mix of expertise, innovation, and capacity makes us the perfect choice to bring your new project to market.

A variety of microencapsulation techniques are widely used in the pharmaceutical industry including fluid bed coating, spray drying, solvent evaporation, and more. However, one method—coacervation—offers several unique benefits to developers interested in working with challenging and/or bitter-tasting molecules, managing a product’s lifecycle, and accelerating development timelines. Learn how Adare’s Microcaps® taste masking technology platform, utilizes the coacervation process to solve your formulation challenges.

Discover why integrating Human Factors and patient activities from early device to manufacturing is essential to develop a patient-centric inhaler.

CPI, a CDMO specializing in Wurster fluid bed coating, has designed and optimized equipment based on linear scaling principles, creating ease and predictability to scale-up.

Nitrite determination in the USP monograph was evaluated with a Dionex IonPac AS15 column using an ICS-5000 HPIC IC system according to the Dalteparin Sodium monograph.

Not all water is equal. This white paper will explore why. It dissects what water activity is, why it’s critical in battling microbes, and lists growth-limiting aw levels for common microorganisms.

Modular cleanroom construction can offer a number of important advantages over conventional (stick-built) approaches. Learn more about the benefits of modular here.

Specializing in oncology, anti-infective and complex formulations, Pfizer CentreOne provides end to end services from development through to commercial manufacture of sterile dosage forms.

Reviews critical stages of rotary tablet press process, describes impact of multi-tip punches, and how to overcome common challenges in the tablet compression industry

Learn how to develop a robust validation package that supports cell and gene therapy products and their unique features – access our whitepaper.

CROMA continuous coater brings an innovative technological progress in manufacturing based on modularity and truly continuous film coating of tables.

This whitepaper highlights six key points that pharmaceutical companies should consider when selecting the ideal partner to synthesize an API for them.

This white paper describes the challenges in terminal sterilization of parenteral drugs, defines the most important requirements, and offers first-hand solutions.

All drug products have to undergo sterility testing to comply with Good Manufacturing Practices (GMP). Parenteral drug products go through especially rigorous testing to ensure sterility and safety.

After a disruptive year in the pharma industry, it’s time to adapt to the next normal. Learn about the four main trends shaping the evolving industry.

This article will discuss pharmaceutical package testing specifically Helium leak detection technology and how it solves cold supply chain challenges of today’s high-risk pharmaceutical products.  This article also addresses the importance of phase appropriate leak testing from manufacturing through product lifecycle.

Whether at the research and development stage, or manufacturing, the inVia Raman microscope offers simple and fast transmission Raman analysis

This article discusses the benefits and advantages of liquid-filled hard capsule manufacturing from formulation, development and full-scale production

In this white paper, you will learn more about the sizing of the temperature control units for use on various reactor systems to achieve optimal results.

This application note demonstrates how to develop an analytical HILIC method and transfer it from an Agilent 1260 Infinity LC system to the Vanquish Core HPLC system.