Process manufacturers will learn how to transition their facility to a more efficient, data-driven production environment by learning and embracing the five components of a modern-day Smart Factory.

How can you improve safety and compliance during pH calibration? This whitepaper provides expert tips for accurate and consistent measurements. Learn best practices to maintain buffer integrity, uphold quality control, and meet regulatory standards.

Discover how to build a modern, secure and scalable physical access control system—for doors, devices and more—using RFID and mobile credentials.

Explore how RFID and mobile credentials enable secure, phishing-resistant user authentication that supports compliance with evolving cybersecurity standards.

Learn how to enhance security and usability in SSO environments with passwordless, phishing-resistant authentication based on RFID and mobile credentials.

Access control is evolving, requiring flexible and future-proof solutions. Learn how universal readers support multiple technologies, ensure seamless integration, and simplify authentication—helping businesses stay secure, adaptable, and efficient.

Secure and reliable machine authentication provides manufacturers with essential data for process and workforce optimization. Learn why "who" matters in machine operation and how authentication enhances quality control, cost efficiency and safety.

User authentication and access control are essential for the modern, connected factory. Discover how intelligent manufacturers use smart, unified access systems to enhance security, boost productivity, and optimize workforce and production.

Wet granulation of pharmaceutical granule mixtures with subsequent fluid bed drying represents the most important step in the production of solids. You can find out which other processes you should know here.

Specialisation, small product quantities and fast production cycles in granulation require pharmaceutical manufacturers to think of adaptive plant technology. The whitepaper reveals what is key to keep your production of solids flexible.

In the China Biopharmaceutical Industry Report, the analysts provide insights into recent market developments and current conditions and highlight the industry's opportunities and challenges.

Download the Compliance Guide containing 18 FAQ to learn how to ensure adherence to the European Pharmacopoeia (Ph.Eur.) Chapter 2.1.7 "Balances for Analytical Purposes".

The efficiency of a fermentation process in pharma or food production often remains unchallenged for years, unless there are acute issues. The white paper gives insights on how to use Artificial Intelligence to improve this process.

According to market research, the market volume for "green" chemistry is due to almost double by 2025. Our white paper sets out how contract manufacturers are reacting to the trend for sustainability.

This paper will show by means of the example of a pusher centrifuge how to achieve optimum product quality, maximum energy efficiency and operation with a minimum of downtime and it describes the most important innovations of the past decade.

This paper looks at how the earlier PTA production method involving a multi-stage process with pressure and atmospheric centrifuges and a re-slurry tank can be replaced with one stand-alone device – the rotary pressure filter (RPF).

Do you want to operate radiometric measurements with minimal uncertainties to allow optimum performance of your process? Minimize error sources, so that difficult level, density & bulk flow measurement tasks achieve highest accuracy & reproducibility

RE100 companies have blazed a trail, but it's the next wave of corporates who need to start their journey if we are to reverse climate change. What are the opportunities? What are the barriers and how can they be overcome? What options are available?

The situation for contract manufacturers is challenging. Operating in a highly competitive market, companys have to transform challenges into opportunities. The white paper describes the situation of this particular industry and survival strategies.

When developing new products, the design validation may cause high pressure. With a prototype, designers can transform virtual designs into physical, manageable parts.

The white paper discribes a new bottom-mounted magnetic agitator for aseptic mixing processes of high volume cell cultures in bioreactors up to 30,000 liters.