For 42 years, INTERPHEX has proven to be the place to find all of the state-of-the-art solutions you need to cost-effectively develop and manufacture quality products. INTERPHEX is the premier pharmaceutical, biotechnology, and device development and manufacturing event to experience science through commercialization.
445 11th Avenue
New York, NY, 10001
May 24, 2022: 10:00 am – 5:00 pm
May 25, 2022: 10:00 am – 5:00 pm
May 26, 2022: 10:00 am – 1:00 pm
All aboard! Your Automation Journey Begins Here!
Catherine Thacker, Director Life Sciences Marketing,
Is your product suitable for automated manufacturing? Has your R&D team defined the product and process requirements to the point where you can author a detailed user requirements specification? Have you identified the in-process critical-to-quality attributes that you want to address with automation? How does the product demand forecast influence your manufacturing and automation plan? When is the right time to kick-off an automation project? Attend our session about planning for automation. We will share best practices for establishing a manufacturing strategy and building your business case, putting you on track to your final destination successful delivery of your project.
May 24, 2022: 11:00 am
May 25, 2022: 2:00 pm
May 26, 2022: 11:00 am
Emerging Technologies in Assembly Automation
Albert Kleinikkink, Director R&D, P. Eng., MBA
Pharmaceutical manufacturing systems operate inside of demanding constraints, but innovations are providing new opportunities to drive efficiencies and re-imagine these manufacturing systems. In this session, we will explore the state of the art in two such technologies – material conveyance in aseptic environments, and LED UV-curable adhesive processes for medical devices.
May 24, 2022: 12:00 pm
May 25, 2022: 3:00 pm
May 26, 2022: 11:30 am
Quality by Design (QbD) is expected by regulatory agencies, and rationalization will be required if this philosophy is not adopted. Creating QbD is made easy with the Process Analytical Technology (PAT) tools available within the SP Line of Sight™ (LoS). Understanding your process design space will ensure that your products maintain the quality required for patient safety. Managing deviations is one of the most laborious activities, putting your batch at risk for potential reject, and requiring extensive effort for rationalization to support acceptance, especially for lyophilized products. It impacts your business bottom line and triggers red flags for your products’ annual report and inspection. This presentation will help you prepare your organization for those events when data to support your product quality will be needed. We will discuss the benefit of QbD and the data you obtain through the LoS approach for batch recovery.
May 24, 2022: 1:00 pm
May 25, 2022: 11:00 am
May 26, 2022: 12:00 pm
The presentation will cover this topic by giving an overview of combination products and how they are used in the pharma industry, highlighting advantages and disadvantages and sharing views from different angles. After this preliminary introduction, the presentation will focus on a particular type of device for Aseptic Ready-to-Mix combination products, showing case studies on how this innovative technology can be safely handled in aseptic processing.
May 24, 2022: 2:00 pm
May 25, 2022: 12:00 pm
May 26, 2022: 12:30 pm
We will explore what a Lyobead is, what benefits they offer over traditional forms of pharma and reagents, and how we create them. We will take a quick visual tour of BioDot dispensing and nitrogen wells, SP and Lyophilization and then talk about some adders such as automated handling, loading and aseptic enclosures.
May 24, 2022: 3:00 pm
May 25, 2022: 1:00 pm
May 26, 2022: 10:30 am