ISPE
International Society for Pharmaceutical Engineering
ISPE provides education, training, forums, and technical documents for professionals in pharmaceutical manufacturing. The Society publishes best-practice guides on a wide array of topics, including bulk pharmaceutical chemicals, sterile manufacturing facilities, commissioning and qualification, biopharmaceutical manufacturing facilities, and technology transfer.
Top Sellers:
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ISPE GAMP Good Practice Guide: A Risk-Based Approach to Operation of GxP Computerized Systems – A Companion Volume to GAMP 5 PDF
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ISPE Baseline Guide: Volume 5 – Commissioning and Qualification, 2nd Edition PDF
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ISPE Baseline Guide: Volume 2 – Oral Solid Dosage Forms PDF
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ISPE GAMP 5: A Risk-Based Approach to Compliant GxP Computerized Systems, Second Edition PDF
New Revisions:
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Good Practice Guide: Knowledge Management in the Pharmaceutical Industry PDF
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ISPE Sustainability Handbook PDF
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ISPE Baseline Guide: Volume 6 – Biopharmaceutical Manufacturing Facilities PDF
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ISPE Guide Series: Product Quality Lifecycle Implementation (PQLI) from Concept to Continual Improvement Part 4 – Process Performance and Product Quality Monitoring System PDF
Explore More in ISPE
Showing 17–32 of 65 resultsSorted by latest
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ISPE Good Practice Guide: Harmonizing the Definition and Use of Non-Investigational Medicinal Products (NIMPs) PDF
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ISPE Baseline Guide: Volume 1 – Active Pharmaceutical Ingredients (Second Edition) PDF
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ISPE Good Practice Guide: Process Validation PDF
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ISPE GAMP Good Practice Guide: Computerized GCP Systems & Data PDF
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ISPE Good Practice Guide: Process Gases PDF
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ISPE Good Practice Guide: Maintenance PDF
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ISPE Guide: Cleaning Validation Lifecycle – Applications, Methods, & Controls PDF
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ISPE GAMP Good Practice Guide: A Risk-Based Approach to Operation of GxP Computerized Systems – A Companion Volume to GAMP 5 PDF
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ISPE Good Practice Guide: Good Engineering Practice, Second Edition PDF
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ISPE Baseline Guide: Volume 7 – Risk-Based Manufacture of Pharmaceutical Products (Risk-MaPP) PDF
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ISPE Guide Series: Product Quality Lifecycle Implementation (PQLI) from Concept to Continual Improvement Part 3 – Change Management System as a Key Element of a Pharmaceutical Quality System PDF
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Good Practice Guide: Investigational Medicinal Product Reverse Logistics PDF
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ISPE Good Practice Guide: Approaches to Commissioning and Qualification of Pharmaceutical Water and Steam Systems PDF
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GAMP Good Practice Guide: A Risk-Based Approach to GxP Process Control PDF
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ISPE Good Practice Guide: Continuous Manufacturing of Oral Solid Dosage Forms PDF
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ISPE Good Practice Guide: Asset Management PDF