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Helping to speed your product to market and gain efficiency

Content provided by Colorcon Inc. | 22-May-2018 | Data Sheet

With a commitment to provide best-in-class solutions, Colorcon's Solid Dose newsletter brings you the latest insight to support your development and...

Next generation ePRO from SQN Health

Content provided by Syne Qua Non Clinical | 16-May-2018 | Business Advice

In an era of rapid technology growth, healthcare requires low cost solutions for real-time data collection. We have come a long way from paper to EDC and...

Customized Fill Release in Gelatine Soft Capsules

Content provided by Gelita AG | 07-May-2018 | Application Note

From rapid release in the stomach for e.g. analgesics to enteric release for fills with unpleasant aftertaste – GELITA delivers the respective gelatine...

Sterile Injectables Contract Manufacturing

Content provided by Baxter BioPharma Solutions | 02-Apr-2018 | Product Brochure

Baxter BioPharma Solutions' award-winning facility in Bloomington, Indiana, USA, is a leader in sterile contract manufacturing of injectable products.

Lyophilization Scale-Up and Tech Transfer

Content provided by Baxter BioPharma Solutions | 12-Mar-2018 | White Paper

There are few challenges when increasing the scale of production for a solution formulation, but the challenges drastically increase when the formulation...

How will Brexit affect the Pharmaceutical Industry?

Content provided by Source BioScience Ltd | 08-Mar-2018 | White Paper

Have you prepared your strategy for the outcome of Brexit to ensure that you can continue to supply the UK market?
Source BioScience is a CRO with...

Strategies to Select and Deliver the Right Candidate

Content provided by Catalent | 05-Mar-2018 | White Paper

Does your candidate have what it takes to succeed? Do you have the information needed to make the right decisions about your candidate’s path to the clinic?...

Leveraging Best Practices in Primary Packaging

Content provided by Catalent | 05-Mar-2018 | White Paper

When planning a clinical trial, overlooking the importance of primary packaging can be a mistake. From stability concerns to labeling to patient compliance...

NEW…sugarcane derived USP Squalane from Aprinnova

Content provided by APRINNOVA – A joint venture of AMYRIS and NIKKOL Group | 26-Feb-2018 | Product Brochure

To date, topical formulation chemists have been restricted to using Squalane derived from the harvesting of shark livers. Neossance Squalane USP, derived...

Roquette Oral Dose Case Study - Part IV

Content provided by Roquette Pharma Solutions | 04-Dec-2017 | Case Study

Download the latest Roquette case study and learn more on how PEARLITOL® Flash mannitol and starch compound offers inert stability, fast disintegration...

Roquette Oral Dose Case Study - Part III

Content provided by Roquette Pharma Solutions | 27-Nov-2017 | Case Study

Download the Case Study to find out how Roquette’s SweetPearl® P 300 DC maltitol technology makes an effervescent tablet solution attractive and palatable...

Meet the challenges of complex injectables

Content provided by Vetter Pharma International GmbH | 07-Nov-2017 | White Paper

In the time it takes from the exciting discovery phase to the rigorous demands of a commercial launch, unexpected scientific and technical challenges can...

The Solid Dose, Latest News from Colorcon

Content provided by Colorcon Inc. | 06-Nov-2017 | Data Sheet

With a commitment to serve customers through product innovation and technical excellence, Colorcon's Solid Dose newsletter brings you the latest insight...

Roquette Oral Dose Case Study - Part II

Content provided by Roquette Pharma Solutions | 06-Nov-2017 | Case Study

Download the case study and learn more on how Roquette’s taste masking technology KLEPTOSE® Linecaps (KL) allows the delivery of an efficient taste masking...

Roquette Oral Dose Case Study - Part I

Content provided by Roquette Pharma Solutions | 06-Nov-2017 | Case Study

Download the Case study and learn more on ReadiLYCOAT®: Immediate release film coating system for heat sensitive oral dosage forms is a breakthrough in...

Process Development for Lyophilized Products

Content provided by Baxter BioPharma Solutions | 30-Oct-2017 | Application Note

Baxter approaches formulation and process development with the intention of identifying the failure points for the product. Knowing where the product fails...

Why managing variability?

Content provided by SIO/ADM | 02-Oct-2017 | Research Study

Significant efforts are necessary to develop an active pharmaceutical ingredient (API). It is therefore risky to expose this API to poorly characterized...

Optimizing vessel geometry for mag drive agitators

Content provided by Steridose, Inc | 14-Sep-2017 | White Paper

The performance of a bottom mount magnetically driven agitator (mag drive mixer) is heavily dependent on its relationship with the vessel’s geometry, baffles,...

Advancing therapeutics for myeloma

Content provided by Recipharm AB | 04-Sep-2017 | Case Study

Multiple myeloma is the second most common blood cancer in the world and despite survival rates increasing over the last decade, there remains a requirement...

Enabling drug traceability. Implementing serialization in practice as a CDMO.

R-Pharm Germany GmbH | Recorded the 10-Oct-2017 | Webinar

R-Pharm Germany has established an effective track & trace system to meet all regulatory requirements and to offer cost-effective and customer-oriented...

GELITA® Gelatine for State-of-the-Art Delivery Systems

Content provided by Gelita AG | 21-Aug-2017 | White Paper

The latest development of the GELITA Competence Team is GELITA® RXL R2 that takes the reduced cross-linking (RXL) concept provided by GELITA® RXL one step...

Survey Report: State of the Global Pharmaceutical Contract Services Industry 2017

Content provided by William Reed | 27-Jul-2017 | Application Note

In May 2017, Outsourcing-Pharma.com conducted its inaugural “state of the industry” survey of its user base of pharmaceutical industry professionals, including...

How to get reproducible DNA amplification

Content provided by Eppendorf Bioprocess Solutions | 27-Jun-2017 | Infographic

DNA concentration, mastermix preparation, temperature management: Doing PCR like a pro can be more complex than it seems.The Eppendorf infographic helps...

Influence of Different Lubricants on Tableting Characteristics and Dissolution Behavior

Content provided by JRS PHARMA | 14-Jun-2017 | Application Note

Apart from their desired effect of reducing the ejection force and punch adhesion, lubricants also have a considerable influence on the tablet hardness,...

Increase tablet production with multi-tip tools

Content provided by I Holland Limited - Tabletting Science | 01-Jun-2017 | White Paper

Multi-tip punches increase the number of tablets produced per turret rotation, which increases production rates of existing presses.This tooling has transformed...

Selecting a dosage form for delivery to the lungs

Content provided by Recipharm AB | 15-May-2017 | White Paper

Selecting and developing an appropriate dosage form for inhalation products can be challenging. The physicochemical properties of the API, the required...

First-in-Human Development Strategies

Content provided by Catalent | 01-May-2017 | Insight Guide

Crucial and cost-effective factors to consider when transforming a pre-clinical development compound into a first-in-human, early-phase drug candidate....

Free Infographic: Stem Cell Expansion in Bioreactors

Content provided by Eppendorf Bioprocess Solutions | 28-Mar-2017 | Infographic

To produce large numbers of stem cells in consistent quality, bioreactors offer many advantages over dishes and flasks. However, switching the culture...

The Power to Make, A Virtual Tour

Content provided by Althea | 24-Mar-2017

You have the power to make a difference. To make new therapeutics that improve quality of life and inspire a healthier world. To do this, you need a manufacturing...

Cleaning Validation - What do you need to consider to ensure a successful outcome?

Content provided by RSSL | 22-Mar-2017 | White Paper

The data used to determine the success of a cleaning validation is built upon both the effective evaluation of the manufacturing plant and the robustness...

Taking fill release rates to a new level

Content provided by Gelita AG | 20-Mar-2017 | White Paper

Various attempts by the pharmaceutical industry to reduce cross-linking with additives have only been partially successful. GELITA, however, followed another...

psiXchange - Innovating SUSAR Distribution

Content provided by pharmasol | 20-Mar-2017 | White Paper

A controlled document distribution process, in which getting the right information to the intended recipients within a required time frame and being able...

Serialisation – know the facts

Content provided by Recipharm AB | 20-Mar-2017 | Product Presentation

The EU and US deadlines for serialisation are looming and pharmaceutical companies need to be prepared in order to ensure compliance. Implementing serialisation...

Dissolving boundaries in worldwide clinical trial logistics

Content provided by Marken | 15-Mar-2017 | Competition

Marken maximizes efficiency and enhances service offerings while continuing to specialize in the high-touch, personalized services that the company is...

HOW TO MAXIMISE TOOLING LIFE SPAN & PRODUCTIVITY THROUGH PLANNED PROFESSIONAL MAINTENANCE

I Holland Limited - Tabletting Science | Recorded the 02-Mar-2017 | Webinar

Tablet punches and dies are often viewed as consumable items that can be replaced at relatively low cost. However, with the constant challenge of increased...

VALSYNTHESE – Custom phosgenation under GMP

Content provided by Valsynthese SA | 01-Mar-2017 | White Paper

Phosgene is a powerful reagent allowing the straightforward synthesis of key intermediates such as chloroformates, acid chlorides, and carbamoyl chlorides....

See How Demand Led Supply Can Improve Supply Chain Flexibility

Content provided by Catalent | 23-Jan-2017 | White Paper

Clinical trials are more complex than ever before, driving the industry to develop and adopt new ways to manage clinical supplies and address new challenges.Fast...

Producing the perfect soft gel

Content provided by Leading manufacturer of gelatine and collagen peptides | 17-Jan-2017 | White Paper

This white paper outlines the key considerations to ensure gelatin is enhanced for soft gel formulation, efficient gel production and optimal API delivery...

Nemera: Using intelligent design to deliver safe preservative free multi-dose eye drops

Content provided by Nemera | 12-Dec-2016 | White Paper

Novelia® represents a major innovation in ophthalmic drug delivery by providing a preservative-free alternative for chronic treatments in a patient-friendly...

Patient-Centric Drug-Development Process

Content provided by Catalent | 28-Nov-2016 | Insight Guide

For large and small pharmaceutical companies alike; developing a new drug is fraught with risk. Patient-centric drug development and optimization is both...

Critical Supply Strategies for Biologic/Biosimilar Studies

Content provided by Catalent | 22-Nov-2016

As more approved biologics near patent expiration, the race to be first to market with a biosimilar alternative will intensify. Delays encountered during...

Choosing the Right Size Sphere

Content provided by Colorcon Inc. | 21-Nov-2016 | White Paper

Choosing the right size sugar sphere, for a multiparticulate dosage form is imperative. Size matters; not only to achieve a robust formulation and efficient...

Tailoring the autoinjection with SAFELIA®

Content provided by Nemera | 21-Nov-2016 | White Paper

For a better patient experience and for an optimized drug deliver, including for high volumes high viscosities formulation.Safelia injection course can...

Experience foam for topical drug delivery

Content provided by Gattefossé | 14-Nov-2016 | White Paper

Pharmaceutical foams are becoming more popular probably due to more topical medicines being switched to OTC and the need to innovate and differentiate...

Elemental Impurities Regulations View from a CRO

Content provided by RSSL | 02-Nov-2016 | White Paper

Regulatory control of elemental impurities in pharmaceutical products has long been discussed, with both the European Pharmacopeia (EP) and the United...

Healthy and suitable for all types of patient, SweetPearl® or LYCASIN® is what you need!

Content provided by Roquette Pharma Solutions | 25-Oct-2016 | Product Brochure

The quality and stability of your formulations is your ultimate challenge.Whether you need the optimal diluent for your solid dosage forms or the ideal...

Challenges and SEPPIC solutions for moisture sensitive formulation

Content provided by SEPPIC | 24-Oct-2016 | White Paper

One of the challenges of the formulators is to develop stable formulations which protect API from moisture. To find solutions and different ways of protecting...

NXT LVL Clinical Trials. Direct-to-Patient: Your Top 10 Q&A.

Content provided by World Courier | 10-Oct-2016 | White Paper

Take your clinical trials to the next level. The direct-to-patient (DtP) model solves two of the largest issues plaguing clinical trials: patient recruitment...

pH measurement: Six technical tips

Content provided by Metrohm – customized analysis for the pharmaceutical industry | 10-Oct-2016 | White Paper

The pH value is one of the most important and therefore also one of the most frequently measured quantities in analytical chemistry. Sometimes a simple...

A unique pharmaceutical oil for solubility and oral bioavailability enhancement

Content provided by Gattefossé | 01-Oct-2016 | White Paper

This white paper features Maisine® CC, Gattefossé’s tradename for glyceryl monolinoleate (USP-NF), also known as corn oil mono-, di- and triglycerides....

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