ISPE Guidance Documents by Topic

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Active Pharmaceutical Ingredients

Biotechnology

Commissioning and Qualification

Containment

Critical Utilities

Disposables

Engineering Standards Benchmarking

Good Automated Manufacturing Practice (GAMP®)

Good Control Laboratory Practices

Heating, Ventilation, and Air Conditioning

Investigational Products

Operations Management

Oral Solid Dosage

Packaging

Process Analytical Technology (PAT)

Process/Product Development

Project Management

Sterile Products Processing (SPP)

Sustainable Facilities

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Design Considerations for WFI Distillation Systems Part 4
Thursday, 26 May 2016 13.05

Direct Access to Quality Manufacturing Experts
Wednesday, 25 May 2016 13.05

Broadening Pharmaceutical Training Footprint in Europe
Tuesday, 24 May 2016 19.05