Continuous Pharmaceutical Processing and Process Analytical Technology 1st Edition

Continuous Pharmaceutical Processing and Process Analytical Technology, 1st Edition (by) offers a timely, practical guide for professionals navigating the shift from batch to continuous manufacturing. Whether you work in R&D, process development, quality assurance, regulatory affairs, or production, this book illuminates the technologies and strategies reshaping modern pharmaceutical manufacturing.

Begin with a clear overview of continuous processing principles and the role of Process Analytical Technology (PAT) in enabling real-time monitoring, robust process control, and faster product release. The text bridges fundamentals and application—covering process design, sensor selection, data analytics, scale-up challenges, and regulatory considerations—so you can translate theory into reliable, compliant operations.

Packed with industry-focused insights and practical frameworks, this title demonstrates how continuous approaches improve efficiency, reduce waste, and support Quality by Design (QbD). Examples and case studies reflect global regulatory expectations and manufacturing practices across the US, EU, and Asia-Pacific, making the content relevant to multinational teams and regional manufacturers alike.

Readable yet authoritative, the book equips engineers, scientists, and decision-makers with the know-how to implement PAT-enabled continuous processes and to communicate value to stakeholders. If your goal is to modernize production, lower cost of goods, and accelerate time-to-market, this essential resource charts a clear path forward.

Add Continuous Pharmaceutical Processing and Process Analytical Technology to your professional library today and start advancing your manufacturing capabilities with confidence.

Note: eBooks do not include supplementary materials such as CDs, access codes, etc.