Whitepapers

Making an effective vaccine faces obstacles which depend on a complete line-up of pharmaceutical-grade refrigerators and freezers to maintain the necessary conditions.

A significant advantage of MMTS™ Multi Mini Tablet System is the ability for patients and caregivers to open capsules and sprinkle the contents on soft foods.

Pressure for innovative products is becoming greater for pharmaceutical companies as they spend a significant amount on R&D and ways to achieve ROI in biopharma labs.

A testimonial from The National Center for Global Health and Medicine BioBank in Japan, a biobank to help develop leading next generation medicine and drugs.

A testimonial by The Inserm Unit, Institute of Regenerative Medicine Biotherapy (IRMB) in France, a facility dedicated to stem cell research and immunotherapy.

How 50 years of R&D and customer collaboration have contributed in the manufacturing of microbiological incubators to meet emerging applications in biopharma industry.

As biological products are being investigated as treatment modalities, measures to ensure safety and quality from microbiological contamination becomes imperative.

Companies looking to implement a quality management system (QMS) are faced with a dilemma: They can design a custom system from scratch or invest in purpose-built software. Before you decide which kind of QMS is the best fit for your needs, learn the pros and cons of each.

The catch-and-release platform Peptide Easy Clean, developed by Belyntic in collaboration with Bachem, enables the successful and innovative purification of peptides.

The pressure for innovative products is becoming greater for pharmaceutical companies as they spend a significant amount on R&D in all stages of clinical trials. Thus, optimizing efficiency becomes imperative.

As the biopharmaceutical industry gains momentum and biological products are being heavily investigated as treatment modalities, measures are needed throughout to ensure their overall safety and quality from microbiological contamination.

The changes during biopharmaceutical manufacturing, processing and storage can impact the safety and efficacy of products during clinical use. Controlling such product variability is a challenge to maintaining batch-to-batch consistency.

Assuring sample integrity and security during the development, manufacturing, and supply of biopharmaceuticals is one of the most important aspects leading to establishing standards that guarantee proper sample security.

This application note demonstrated an early placement of our ‘in-house’ developed rheological test in the preformulation studies to select right type and amount of lubricant in the formulation, and, if necessary, the desired coating of punches.

Explore how next-gen QMS delivers digital transformation by seamlessly connecting enterprise-wide systems, processes,, documentation, and data in a cost-effective manner

In this white paper we look at reverse engineering existing drug products using Raman imaging.

This white paper discusses developing optimal platform analytical methods with partner CDMOs for effective process impurities clearance in biological drug substances.

Companies looking to implement a quality management system (QMS) are faced with a dilemma: They can design a custom system from scratch or invest in purpose-built software. Before you decide which kind of QMS is the best fit for your needs, learn the pros and cons of each.

This technical bulletin discusses major regulatory updates, introduced by the FDA and EMA, regarding nitrosamines and SGS proposed risk assessment method for compliance.