whitepaper
Whitepaper: Perform conductivity measurements in compliance with USP <645>
“Water is the most widely used substance, raw material, or ingredient in the production, processing and formulation of compendial articles...”
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QA/QC
whitepaper
Application Note: Stearates verification using a handheld Raman analyzer
In this application, a Principal Component Analysis (PCA) method was found to be successful in identifying the various stearates...
news
INTEGRA highlights benefits of low retention pipette tips
INTEGRA has released an application guide highlighting the importance of choosing the right disposable tips for the liquid you’re pipetting...
whitepaper
Whitepaper: Key to outsourcing method development and validation: A pragmatic approach
In an industry that is seeing an increasing level of work being outsourced, the Contract Research Organisation (CRO) of choice needs to have proven experience in both the pragmatism and flexibility of the method developer’s mind set and a regulatory background in validation...
news
Wickham Laboratories announces expansion of media preparation facilities
Wickham Laboratories expands capacity for in-house media preparation...
article
The importance and efficacy of epigallocatechin and epicatechin
Plant extracts have been used in African folk medicine to treat a wide array of infections, especially in Nigeria, for centuries. This article considers the potential medicinal uses and efficacy of the flavonoids epigallocatechin and epicatechin, which can be extracted from the Spondias mombin plant.
article
Determination of glucosamine in food supplements by HILIC-ESI-MS
Glucosamine is sold as a food supplement worldwide, but its production is poorly regulated. A direct and reliable method for the quality control of glucosamine in commercial products is of great importance. This article describes a simple, fast and validated ultra-performance liquid chromatography-quadrupole time of flight (UPLC-QToF) for the determination…
article
Issue #5 2017 – Digital Version
In this issue: Sample preparation - is it possible to have too much? Developing successful over-the-counter syrup packaging for the highly regulated EU market. In-line process PAT in continous wet granulation, and much more...
news
KENX announces CQV – Commissioning, Qualification and Validation University set for Dublin, Ireland
Validation University offers a customisable, hands-on training for immediate, actionable results.
news
BioPure Q-Clamp is compatible with a wide range of connector geometries
The latest innovation from Watson-Marlow Fluid Technology Group brand BioPure is the Q‑Clamp, a new sanitary Tri-Clamp® for single-use fluid path applications...
news
KENX announces Computer Systems Validation and Data Integrity Compliance Congress set for Dublin, Ireland
The CSV and Data Integrity Compliance Congress offers customisable, top-notch training for FDA compliance challenges.
news
Quality control method to select effective MβCD in Neimann-Pick disease
Researchers have developed a quality control method to evaluate the pharmacological activity and potential effectiveness of different preparations of the therapeutic agent MβCD...
editorial-board
Paul G Royall
12 September 2017 | By
Senior Lecturer in Pharmaceutics at King's College London
news
Methodology developed for assessing the value of new medicines
The Advance Value Framework has addressed the pitfalls of current approaches assessing the value of new medicines...
article
Compressed gases: an important component of an environmental monitoring programme
The quality attributes of manufactured pharmaceutical products include the physical, chemical, and microbiological characteristics of the raw materials, excipients and active pharmaceutical ingredient (API), as well as the final drug product (see Table 1). Absence of microbiological contamination is considered a critical quality attribute due to its potential to dramatically…
