Innovations in pharmaceutical Manufacturing Including Capsuling, Tabletting, Additive Manufacturing, Biomanufacturing Operations
Discover how natoli engineering empowers the pharmaceutical industry with innovative equipment, expert training, and unparalleled customer support and expertise. We are the global leader in tablet compression tooling. Our commitment to the tablet compression industry is demonstrated through the development of groundbreaking solutions and progressive, continual improvements in our manufacturing processes. Partner with us – we are better together!
What are some leadership and human resource strategies critical to success in the pharma cdmo sector, including best practices, emerging trends and challenges in managing talent within a highly competitive and evolving industry?
Batch manufacturing has been the standard in the pharma industry, however continuous manufacturing is now proving to be the better choice for efficiency, as well as waste and cost reduction. How can new technologies improve this method further?
In the fast-paced world of pharmaceutical manufacturing, efficiency and precision are non-negotiable. For manufacturers dealing with difficult-to-encapsulate powders and formulations, the Natoli NCF-45 Capsule Filling Machine emerges as a game changer. With the potential to pay for itself in the powder you’ll save, the NCF-45 isn’t just a machine, it’s an investment in better yields and greater profits. Better yields = better profits
There are usually two parameters important to pharmaceutical manufacturers: time and money. Is everything still on schedule? And are they still on budget? They need non-stop insight
Focusing on regulation within pharmaceutical manufacturing can help re-centre a company’s priorities, while ensuring compliance. This can be aided by the use of advanced monitoring techniques
Following good manufacturing practices (GMP) is crucial for stability testing. The analytical data generated from stability studies is a pivotal part of a regulatory dossier submission to substantiate the shelf life claimed for the drug product or drug substance and further support that shelf-life post-approval. All aspects of the stability study must be executed to the highest level of quality to ensure...
Protein-based immunotherapies, such as monoclonal antibodies and adoptive cell transfer therapies, are reshaping oncology treatments, but ensuring their safety and efficacy is crucial for their success
Medical devices should be designed with an awareness of the challenges of a specific disease as well as an awareness of equality, and the uk government has recently produced a new initiative around this, but how will this impact medical device production going forward?
Protein synthesis is the process by which cells build proteins, fundamental molecules necessary for virtually all cellular functions, but how can this be used within the discovery and manufacturing of new drugs and how can it be automated?
This article explores the significant opportunities within the biologics contract development and manufacturing organisation (CDMO) industry to optimize client satisfaction by meeting the critical demands of discerning clients. Six key facets are identified as pivotal to success, while underscoring the fundamental role of a client-centric approach and the importance of building and nurturing strong client relationships.
Robots are revolutionising manufacturing, but manual programming hampers their potential. Robot offline programming offers a digital solution, reducing human work hours by up to 80% and ensuring swift task readiness