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FREE WEBINAR: The Danger of Poor Clean Room Investigations

How Blaming Common Root Causes Took Precedence over Comprehensive Trending

When it comes to APIs, don’t just be pure … be chromatography sure

Novasep’s chromatography services will save you money, time … and your reputation

FREE DOWNLOAD: Vacuum Guide for Chemical Applications

The 80+ page guide is a vacuum reference document which you do not want to miss out on

Free webcast: Inhaled Bioequivalence - A Broader View of Product Development

Watch a free informative video by Vectura, register now using the link below

Understanding maximum compression force

Kevin Queensen, Mechanical Engineer Natoli Engineering Company revisits the maximum compression force for various tablet configurations

Introducing Mobius Chrom 20 System from Merck

For purification of clinical and process scale biologics

Tabletability, compactability and compressibility: What’s the difference?

To patients and consumers, tablets are a simple and convenient dosage form, but the science behind compressing a block of particles or granules into a single tablet can be complicated. Here, the tablet experts Natoli explain how to develop tabletability, compactibility, and compressibility profiles

ON-DEMAND WEBINAR: Manufacturing of Highly Potent Sterile Parenterals

The webinar 'Manufacturing of Highly Potent Sterile Parenterals – Mobile Isolator Based Technology' was hosted by Piramal Pharma Solutions in association with <i>Manufacturing Chemist</i>, on 16 September 2020 and is available to watch for free on demand

Paper gives step-by-step protocols for induced pluripotent stem cells

Scientists and cGMP operation managers at Allele Biotechnology have presented a series of step-by-step protocols for manufacturers of iPSC and other types of stem cells with streamlined cleanroom practices for growing clinical-grade cell products

ON-DEMAND WEBINAR: Delivering the added dimension in Scale-up

Watch Jubilant Biosys' complimentary webinar and live Q&A, hosted in association with Manufacturing Chemist on 7 July, 2020

ON-DEMAND WEBINAR: Improved process performance through rapid microbiological detection methods

Charles River's webinar 'Improved process performance through implementation of rapid microbiological detection methods', hosted in association with Cleanroom Technology, is now available to watch on demand

AES free webinar on demand: Conventional vs. Modular Design Build Cleanroom

The webinar, Conventional vs. Modular Design Build Cleanroom – A Clean & Clear Difference, is hosted by Mitchell Gonzales, Vice President of Process Technology and Josh Russell, Director of Project Development at AES Clean Technology

Merck webinar: How to avoid cross-contamination during viable active air sampling in cleanrooms

The webinar will cover the essential points of air sampling units for use in high-grade cleanrooms, along with the requirements for the prevention of cross-contamination

Merck webinar: Environmental monitoring in aseptic isolator manufacturing

Dr Anne-Grit Klees and Tony Ancrum of Merck KGaA, Darmstadt, Germany, are hosting the webinar 'Air Samplers and Media for Biocontamination Control: Environmental Monitoring in Aseptic Isolator Manufacturing' on 12 September

Process control cost savings in the operational phase

Bürkert Fluid Control Systems consider how to reduce process control costs by managing sensors and transducers more effectively

Scaling-up disposable systems for depth filtration in cell culture clarification

Single-use filtration products were conventionally associated with small-scale processes in laboratories; however, biopharmaceutical manufacturers in particular have been keen to extend the advantages to commercial manufacturing with higher total process volumes. The challenge for process engineers is to optimise the separation techniques at their disposal in order to deliver the best technical performance (for example product yield) and acceptable economic performance, while complying with regulatory requirements imposed by the FDA, writes Lynne Deakin, Field Applications Specialist - Purification Division, 3M United Kingdom plc.

Oligonucleotide Characterisation Services case study

Intertek has more than 15 years\' experience of providing comprehensive GLP/cGMP analytical support to clients involved in oligonucleotide development and manufacturing

Outsourcing in the pharma industry – experience, expertise and enthusiasm

Key success factors in fostering and maintaining a long-term strategic partnership

New White Paper demonstrates value of integrating FlowIR data with Vapourtec Flow Commander software

Gives two examples where FlowIR was used as the key inline diagnostic tool to optimise reaction times

Don’t be thrown off balance – safer operations in biofermentation

Achieving high biofermentation API yield in the minimal time necessitates careful, continuous control of a number of state parameters. Mistakes in process management can result in reduced productivity, extended runs, and in the worst cases, loss of an entire batch. This white paper shows how recent developments in process analytics go a long way to simplifying sensor operations and minimising the risk of human error.

New miniature valves reduce energy consumption by 75%

Reducing the energy consumption of small solenoid valves may not seem particularly significant in isolation, but the knock-on benefits of Bürkert’s TwinPower valves can make a surprisingly large contribution to improving sustainability of labs

On-line TOC and ozone measurement for pharmaceutical waters

The quality of pharmaceutical waters used in product manufacturing must meet all International Pharmacopeia regulations. Any out-of-specified conditions must be identified and corrected immediately

Burkert universal control head delivers cost savings through standardisation

Burkert\'s new Type 8681 control head is ideal for applications on valves used in the hygienic processing industries, where it cuts costs for users by virtue of its ability to be fitted to any manufacturer\'s valves. It has a range of adapters that allows it to be fitted to any actuator currently on the market. It also offers the advantages of easy installation and checking.

Derived measurements for Peak TOC and Average TOC

Compendial Pharmaceutical Waters such as Purified Water and Water for Injection are commonly produced and used continuously as part of the pharmaceutical manufacturing process. Because of this process of continuous usage, demonstration of compliance with TOC regulatory requirements and Pharmacopeia guidelines can become challenging

Trending Articles

  1. Manufacturing Chemist Stand Side with Olon Spa We discover what exhibitors at CPHI Milan 2024 are showcasing LIVE!
  2. Tabletability, compactability and compressibility: What’s the difference? To patients and consumers, tablets are a simple and convenient dosage form, but the science behind compressing a block of particles or granules into a single tablet can be complicated. Here, the tablet experts Natoli explain how to develop tabletability, compactibility, and compressibility profiles
  3. Production of pharmaceutical compounds through microbial fermentation Most people’s experience of fermentation will be through its most famous and popular use – the brewing of beer
  4. Understanding maximum compression force Kevin Queensen, Mechanical Engineer Natoli Engineering Company revisits the maximum compression force for various tablet configurations
  5. Manufacturing Chemist Stand Side with Ezi-Dock Systems We discover what exhibitors at Interphex NYC 2024 are showcasing LIVE!

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