Standard Guide for Risk Assessment and Risk Control as it Impacts the Design, Development, and Operation of PAT Processes for Pharmaceutical Manufacture
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Standard Terminology Relating to Process Analytical Technology in the Pharmaceutical Industry
€72.00
Standard Guide for Science-Based and Risk-Based Cleaning Process Development and Validation
Standard Practice for Qualification of Visual Inspection of Pharmaceutical Manufacturing Equipment and Medical Devices for Residues
€94.00
Standard Guide for Application of Continuous Manufacturing (CM) in the Pharmaceutical Industry
Standard Terminology Relating to Manufacturing of Pharmaceutical and Biopharmaceutical Products in the Pharmaceutical and Biopharmaceutical Industry
Standard Practice for Process to Remove Retroviruses by Small Virus Retentive Filters
€58.00
Standard Practice for Calculating Scientifically Justifiable Limits of Residues for Cleaning of Pharmaceutical and Medical Device Manufacturing Equipment and for Medical Devices
Standard Guide on Sampling for Process Analytical Technology
€65.00
Standard Practice for Process Step to Inactivate Rodent Retrovirus with Triton X-100 Treatment
Standard Guide for Design and Maintenance of Low-Temperature Storage Facilities for Maintaining Cryopreserved Biological Materials
Standard Guide for Inventory Control and Handling of Biological Material Maintained at Low Temperatures
Standard Guide for Handling Hazardous Biological Materials in Liquid Nitrogen
Standard Practice for Process for Inactivation of Rodent Retrovirus by pH
