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Next Generation HPMC Capsules: Bioequivalence and Functional Performance

Capsugel | 17-Feb-2016 | Webinar Live Supplier Webinar
Two-piece hard shell capsules made from hydroxypropyl methylcellulose (HPMC) are emerging as an alternative to conventional gelatin capsu...

Probiota 2016 Conference Programme

Probiota | 05-Jan-2016 | PDF Event programme
NutraIngredients’ Probiota is the leading annual event for the global prebiotic, probiotic and the microbiota focused food and pharma ind...

Excellence in Pharmaceutical Analysis

Butterworth | 01-Jan-2016 | PDF Data sheet
Butterworth specialise in Quality Control Analysis, Method Development, Validation & Stability Testing of Raw Materials, API, Finishe...

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

Butterworth | 15-Dec-2015 | PDF Technical / white paper
The International Conference of Harmonisation (ICH) guidance document on elemental impurities, Q3D, reached step 4 in December 2014, mean...

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

Butterworth | 23-Sep-2015 | PDF Technical / white paper
The classic Modified Atmosphere Packaging (MAP) application, in the pharmaceutical industry, uses medical grade nitrogen to purge atmosph...
Enhanced Residual Solvents Analysis: A Practical Approach to Sampling, Delivery, Storage and Analysis.

Enhanced Residual Solvents Analysis: A Practical Approach to Sampling, Delivery, Storage and Analysis.

Butterworth | 12-May-2015 | PDF Technical / white paper
Samplestorage, handling anddelivery are as important in the determination of residual solvents as the analysis itself. This paper provide...
How BASF supports its pharmaceutical customers towards compliance

ICH Q3D Guideline for Elemental Impurities – How BASF supports its pharmaceutical customers towards compliance

BASF SE | 14-Apr-2015 | Webinar On-Demand Supplier Webinar
On December 19, 2014, the Guideline "ICH Q3D - Elemental Impurities" was issued by the ICH, providing a global policy for limi...
The in-PharmaTechnologist Anti-counterfeiting Forum

The in-PharmaTechnologist Anti-counterfeiting Forum

William Reed Business Media | 16-Apr-2015 | Webinar On-Demand Supplier Webinar
Drug counterfeiting: a pharmaceutical industry problemCounterfeiters rely on two things: poorly secured pharmaceutical supply chains; and...
Amino Acid Analysis According to Ph.Eur 2.2.56

Amino Acid Analysis According to Ph.Eur 2.2.56

SGS | 23-Feb-2015 | PDF Technical / white paper
Employing spectrophotometry and liquid chromatography quantitation of Ninhydrin-positive substances achieves 0.05% reporting sensitivity...
A Method to Meet the New Ph Eur Ninhydrin-Positive Substances Requirement

A Method to Meet the New Ph Eur Ninhydrin-Positive Substances Requirement

Butterworth | 03-Feb-2015 | PDF Technical / white paper
The European Pharmacopeia (Ph Eur) is moving away from the historical thin layer chromatography technique for the determination of Ninhyd...
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