Content focuses on the interactions of multidisciplinary functions and discusses the scientific application of experimental design methodologies as part of the product manufacturing process. Individual topics could include formulation, clinical phases, manufacturing, technology transfer, production scale-up, and optimization.
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Evolving China’s Regulatory System in Alignment with ICH
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Using Industry Survey Data to Shape Cell Therapy Facility Design
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ATMP-Focused Online Seminars Educate and Inspire
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There is much that large-scale commercial stem cell therapy processes can adopt from the existing…
Continuous Manufacturing of Small Molecule Drug Substances
The adoption of continuous manufacturing (CM) in the pharmaceutical industry is increasing because…
ISPE Briefs: A Comprehensive Reference for Continuous Manufacturing of OSD
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USP/BIOPHORUM Workshop on Continuous Manufacturing of Biologics
In the interest of understanding the current state of continuous manufacturing for biologics and to…
Removing Regulatory Hurdles for Continuous Pharmaceutical Manufacturing
Continuous manufacturing (CM) challenged regulators’ expectations and regulatory frameworks. This…
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Realizing the promise of any novel viral vector therapeutic depends on the innovator’s ability to…
Process Validation Lifecycle for Packaging Oral Solid Dosage Forms
In August 2017, ISPE published the Discussion Paper “Overview of Packaging Validation for Drug…
Investigator Initiated Trials (IIT) – Considerations and Guidance from the Perspective of Clinical Trial Supplies and GMP
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Biopharmaceuticals: Webinar de treinamento em C> e ATMP Visão geral Este webinar é uma gravação do novo curso de instrutor que é um curso de nível avançado sobre therapies C e Gene T (C>) e Medicamentos de Terapia Avançada (ATMP). O curso também fornece umavisão geral dos componentes mais comuns e estabelecidos que são aproveitados em produtos C> (por exemplo, plasmídeos, mRNA, nanopartículas lipídicas, vetores virais), cobrindo terminologia, processos de fabricação e subsequente caracterização analítica de os componentes fabricados e os produtos terapêuticos. As plataformas de células T…
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GMP Fundamentals: Production & Process Controls
This course offers an overview of Good Manufacturing Practices (GMP) for medical product production and process control. You will learn about GMP compliance, product design and development, process validation, control systems, and quality control procedures. Regulatory requirements, including FDA and international standards, will be covered. Upon completion, you will understand the fundamental principles and practices of GMP in medical product production. Interactive Course: What to Expect CEUs are provided once you achieve an 80% passing grade and complete the evaluation. Buy Now Return to…
GMP Fundamentals: Control of Excipients, Components and Drug Product Containers/Closures
In this course, you will learn about the fundamentals and importance of GMP control in the pharmaceutical industry. Good Manufacturing Practices (GMP), is critical for ensuring the quality, safety, and efficacy of pharmaceutical products. This includes controlling excipients, components, and drug product containers/closures to meet specific standards and requirements, reducing the risk of contamination, degradation, or incorrect formulation. You will gain a deeper understanding of the role of GMP control in maintaining the integrity of the supply chain, and how following GMP guidelines helps…
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Modo de Entrega: Webinar Produtos Biofarmacêuticos: Webinar de Introdução a Grandes Moléculas Visão geral Este webinar é uma gravação do novo curso ministrado por instrutores que introduz os participantes ao desenvolvimento de biofármacos e abordará conceitos que destacam as diferenças entre moléculas pequenas e biomoléculas (moléculas grandes). O objetivo deste curso é fornecer uma compreensão fundamental dos aspectos CMC de produtos biofarmacêuticos, desde o desenvolvimento até à comercialização. Instrutor O que você vai aprender Desenvolvimento de CMC para Produtos Biofarmacêuticos…