Christopher Meissner, CEO of Meissner Filtration Products, on recent industry trends.
Q&A with
Christopher Meissner, CEO of Meissner Filtration Products
PharmTech:
How do you stay abreast of new developments in the industry?
Christopher Meissner
Meissner:
The Internet is a huge boon that really increases our ability to link our clients, our sales teams, and our engineering teams. Of course, this creates challenges in itself just to prevent important developments from being lost in background noise. We mitigate much of this problem with good teamwork and good tools, but at the end of the day there's no substitute for continuous and direct contact with clients.
PharmTech:
Do you see a new industry trend emerging?
Meissner:
As medicines and treatments become more individually focused, and drugs are more specifically targeted, their manufacture increases in complexity, requiring greater levels of safety. Many active pharmaceutical ingredients use chemicals that require extreme efforts to minimize operator exposure, and more efficient methods of managing these processes are required. Product innovations, such as disposable filter assemblies that isolate operators not only from fluid contact, but also from vapor contact when they are changing filters, provide a way in which these chemicals can be handled safely and produced efficiently.
PharmTech:
What is the most common demand your clients are currently making of you?
Meissner:
Custom-engineered solutions for clients often require a significant amount of time for approval. Many times, approval is pushed through only days before product is needed by manufacturing. Our most common request is to expedite the delivery of these developed solutions. In addition, each client often has a slightly different approach for mitigating risk associated with any change, and we see a corresponding increase in requests for new and innovative solutions to meet their approaches.
Navigating Annex 1 for Early Phase Sterile Fill Finish in Clinical Supplies
November 21st 2024Stay compliant with Annex 1 for early phase sterile fill finish processes. Discover how to implement robust contamination control strategies, integrate isolator technology, and conduct integrity testing to meet stringent European Union standards. The guide provides a comprehensive look at key elements such as PUPSIT, critical zone controls, and monitoring and training for aseptic processes.
Why is the PDA Pharmaceutical Microbiology Conference the Hottest Ticket in the Industry?
October 10th 2024Get a glimpse of the power and popularity behind the PDA Pharmaceutical Microbiology Conference from two planning committee members, Julia Marre, PhD (Associate Director, Scientific and Regulatory Affairs at Pocket Naloxone Corp) and Dawn Watson (Executive Director, Global Micro Quality and Sterility Assurance at Merck). This candid conversation reveals why this industry event is so influential…and always sold out! The speakers discuss what makes the PDA Pharmaceutical Microbiology Conference so vital to industry professionals, as well as how to become a part of this dynamic professional community.
Ensuring Quality from the Start: Raw Materials Testing Support
November 21st 2024Raw Materials are the foundation of every biopharma product. Our ultimate guide highlights how our testing support can help you establish purity, identity, and quality standards, ensuring a smooth manufacturing process and adherence to regulatory requirements.
Ensure the Safety of Allogeneic Therapies with Advanced qPCR Testing
November 21st 2024Elevate your viral screening with Eurofins BioPharma Product Testing’s qPCR- based assays. Our advanced testing goes beyond standard screenings to detect even dormant and hard-to-detect pathogens, ensuring comprehensive safety in every stage of the allogeneic therapy pipeline. Protect your products – and your patients- with industry-leading sensitivity and specificity.