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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...

Free On-Demand Webinar: Overcoming Your Rapid Microbial Method Validation Challenges.

EMD Millipore | 03-Dec-2015 | Webinar On-Demand Supplier Webinar
EMD Millipore, the Life Science business of Merck KGaA of Darmstadt, Germany, invites you to join a free, on-demand webinar on ways to ov...

Live Webinar on Recent PAT applications for Softgels presented by Softigel by Procaps

Procaps S.A. | 30-Nov-2015 | Webinar On-Demand Supplier Webinar
Process Analytical Technologies (PAT) in solid dosages forms are commonly used for tablets. Procaps brings to you this webinar inten...

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...
Live webinar on disinfection processes & sampling on sanitized surfaces

Live webinar on disinfection processes & sampling on sanitized surfaces

EMD Millipore | 22-Oct-2015 | Webinar On-Demand Supplier Webinar
This webinar will inform about the Disinfection management in pharmaceutical cleanrooms. The guest speaker Tim Sandle will talk about reg...

Elemental Impurities for ICH Q3D, USP, and EP

SGS Life Science Services | 15-Jun-2015 | PDF Technical / white paper
This white paper describes the risk assessment, implementation, and validation of the new elemental impurity guidelines. In order to meet...
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...
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