Continuous Improvement Through Continuous Manufacturing

In our packed out content sessions at CPHI Barcelona this year we focus on some of the hottest topics coming up in the pharma industry, with each track sponsored by a leading expert in the field. 

This handout highlights how the USP Ingredient Verification Program helps ensure the quality of active pharmaceutical ingredients (APIs).

The USP Ingredient Verification Program helps ensure the quality of excipients by:
- Auditing manufacturing sites for conformance with Current Good Manufacturing Practices (CGMP)
- Testing product samples in laboratories
- Reviewing quality control and manufacturing product documentation
-Monitoring annually with CGMP audits, product reports, and product testing

Understanding the impact of ingredient quality on pharmaceutical companies of all sizes is essential. Join this presentation to dive deeper into ingredient quality trends and solutions available to minimize risk. This presentation will address: Potential impact to pharmaceutical companies concerning recent regulatory trends relating to ingredient quality Supplier qualification process examples at pharmaceutical companies Tools that can assist small and large pharmaceutical companies with reducing supply chain risk and disruptions due to ingredient quality

Most pharmaceutical companies are slowly adopting an electronic method to manage the quality of operational processes and organisational priorities across the value chain. Join us and hear from our expert on how to maximise automation systems in your supply chain. Obtain the quality information you need to discover failures early, and rapidly adjust your production process when needed Automate quality control to process a high volume of samples and reduce human error

The ACS Green Chemistry Institute (GCI) and the pharmaceutical industry are collaborating to advance and facilitate the implementation of research, development, and commercialisation of greener chemistries for a more sustainable pharma industry.
To catalyse tangible green and sustainable chemistry and engineering innovation, the member companies of the ACS Green Chemistry Institute Pharmaceutical Roundtable (ACS GCIPR) have identified, designed, and deeply examined a unique toolbox that includes an array of commonly agreed-upon metrics and tools, widely used by the industry while designing their processes. This session is cover the following: Developing effective accessible tools, including Reagent Guides, an interactive solvent selection tool, a calculator for comparing the environmental impact of analytical methods Assessing current benchmarks of pharmaceutical processes as well as a preview of new tools currently in development

Technology is playing an ever-greater role in life sciences, and new ways of working in automation and supply chain. Join our panel of experts where they will delve into what is required in developing a new standard for manufacturing quality Focus on business and patient outcomes over technology to help identify the right setup Making your data actionable to improve decision-making and real-world automation Identifying the right Enterprise Resource Planning system for your supply chain and manufacturing process Establishing measurable KPIs to better manage and evolve your supplier network based on qualitative and quantitative factors