Excipients, raw materials and intermediates

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.

Specific Excipient Requirements in Continuous Tablet Manufacturing

Content provided by JRS PHARMA | 30-Aug-2022 | White Paper

Continuous Manufacturing Technology continues to gain importance in pharmaceutical manufacturing.

The Effect of Tamping Force on Bi-Layer Tablets

Content provided by JRS PHARMA | 15-Aug-2020 | White Paper

Formulation of bi-layer or multi-layer tablets enables the combination of two or more drugs that may be incompatible or maybe intended for delivery at...

TCC TB - Tricalcium citrate as excipient for direct compression

Content provided by Jungbunzlauer | 05-Nov-2018 | White Paper

TCC TB is a tricalcium citrate tetrahydrate designed to function as a direct compression excipient. It combines exceptional compression characteristics,...

Accelerate your supply chain as pressures intensify

Content provided by William Reed | 17-Sep-2018 | White Paper

Food, Drink and Non-Food manufacturers are under pressure. Range reviews, massive retail mergers, the backlash against plastic packaging and the ongoing...

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...

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...

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...

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...

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,...

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....

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...

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...

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...

Optimise the texture of pharma gel formulations

Content provided by Stable Micro Systems | 31-Oct-2016 | White Paper

Convenient, comfortable and highly effective, gel-based pharmaceuticals are booming. For optimal robustness and efficacy, texture is critical. Discover...

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...

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...

Time and cost savings in pharmaceutical production with high performance equipment cleaning after processing EUDRAGIT® coatings

Evonik Health Care | Recorded the 25-Oct-2016 | Webinar

The cleaning of coating equipment for pharmaceuticals can make up a significant portion of production costs, particularly in commercial-scale processes....

Elemental Impurity Analysis in Pharmaceuticals – The Road To Implementation of ICH Q3D

Content provided by Butterworth | 13-Sep-2016 | White Paper

The International Conference of Harmonisation (ICH) guidance document on elemental impurities, Q3D, reached step 4 in December 2014, meaning the final...

Impact of Extrusion Process Parameters on Drug Recovery and Dissolution

Content provided by Information not available | 04-Jul-2016 | White Paper

This technical paper studies the impact of extrusion process parameters on the performance of solid dispersions of Ritonavir, a poorly soluble antiretroviral...

The Effect of Silicification on the Roller Compaction Performance of Microcrystalline Cellulose

Content provided by JRS PHARMA | 31-May-2016 | White Paper

Roller compaction, or dry granulation, is a manufacturing method for pharmaceutical and nutraceutical tablets that continues to gain importance. In order...

Early development screening for technology selection and formulation design

Capsugel | Recorded the 04-May-2016 | Webinar

In early formulation development of low solubility drugs, it is critical to identify the appropriate technology and produce promising formulations with...

White paper: ensure quality in novel dosage forms

Content provided by Stable Micro Systems | 14-Mar-2016 | White Paper

From oral sprays to pastilles and capsules, pharmaceutical products must increasingly cater for a wider range of preferences. Download this free white...

High energetic and Phosgene reactions in safe hands

Content provided by Valsynthese SA | 01-Mar-2016 | White Paper

Valsynthese, expert in high energetic and hazardous fine chemical production of key intermediates and APIs, is devoted to delivering high quality services...

Tablet Coating at Low Bed Temperatures with a Novel Coating Polymer

Content provided by Roquette Pharma Solutions | 11-Jan-2016 | Case Study

This study shows how to obtain elegant, uniform coatings with zero visible defects and a practical coating solution for heat sensitive products!

Probiota 2016 Conference Programme

Content provided by Probiota | 05-Jan-2016 | Event Programme

NutraIngredients’ Probiota is the leading annual event for the global prebiotic, probiotic and the microbiota focused food and pharma industries and in...

Excellence in Pharmaceutical Analysis

Content provided by Butterworth | 01-Jan-2016 | Data Sheet

Butterworth specialise in Quality Control Analysis, Method Development, Validation & Stability Testing of Raw Materials, API, Finished Product and...

Maltitol in taste masking of acetaminophen chewable tablets: A synergy of combination

Content provided by Roquette Pharma Solutions | 09-Nov-2015 | White Paper

Masking the bitter taste of acetaminophen in chewable tablets is always a challenge, especially in pediatric tablets where formulation possibilities are...

The Solid Dose, Latest News from Colorcon

Content provided by Colorcon Inc. | 28-Sep-2015 | Data Sheet

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

Enhanced Sampling and Calibration Procedures for the Analysis of Residual Oxygen in Nitrogen Purged Pharmaceutical Packaging by GC-TCD

Content provided by Butterworth | 23-Sep-2015 | White Paper

The classic Modified Atmosphere Packaging (MAP) application, in the pharmaceutical industry, uses medical grade nitrogen to purge atmospheric oxygen and...

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