Sterling Pharma Solutions

Activities: Regulatory Pharmaceutical

Trending Articles

  1. Case study: Building an advanced operations of a viral vector facility Anubhav Bhargava from Skanska walks through some of the main challenges and lessons learned from its recent viral vector manufacturing facility build
  2. What is ISO 8 cleanroom classification? Each cleanroom class is denoted by a maximum concentration of particles per cubic meter or cubic foot of air. ISO 8 is the second lowest cleanroom classification
  3. GMP Annex 1: Validation of disinfectants on cleanroom surfaces Published in August 2022, for implementation in August 2023, Karen Rossington from Contec looks at the revised version of EU GMP Annex 1 expanded and clarified the regulatory...
  4. Combustible dust in pharma: An elusive but very real risk Controlling contamination and controlling hazards simultaneously in today's cleanrooms is difficult, sometimes even oppositional. Many operations have serious gaps that are...
  5. L&M Parnaby completes Ghana’s first cleanroom L&M Parnaby has completed the construction of Ghana’s first cleanroom, which will soon produce pharmaceuticals to supply Western Africa

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Related Content

Containment

ADC handling: the whole story of a facility startup

ADCs are hugely cytotoxic and CDMO Sterling Pharma Solutions were well aware of the handling implications when they acquired ADC Bio in 2021. Michael Ruddick from Sterling explains how the company took this in its stride
Regulatory

A risk mitigation approach to detecting and quantifying metals in APIs

If trace quantities of metals are present in active pharmaceutical ingredients (APIs) or final drug products, they have the potential to adversely affect patients, depending on the dose, particularly if the metal is toxic, writes Scott Hugill, Analytical Department Manager for Sterling Pharma Solutions
Manufacturing

Big names announced for leading Pharma and Cleanroom conference

The Cleanroom Technology Conference and Manufacturing Chemist Live collaboration will take place on the 10-11 November. Delegate tickets are currently available
Design & Build

Sterling Pharma to invest $1.5m in US facility expansion

The UK-based global CDMO plans to expand the cGMP production suites, add a non-GMP scale-up production facility, expand its QC lab and increase the North Carolina site’s R&D capacity
Manufacturing

Sterling Pharma CEO: "As API demand rises, we bolster our offering"

Kevin Cook has announced the new cGMP plant is now operational at the UK site

Dr Mathew Minardi joins Sterling Pharma Solutions

Manufacturing

Sterling Pharma Solutions sold

Healthcare investment company GHO Capital has acquired the API manufacturer for an undisclosed sum
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