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Process Validation for Biotechnological Products - US edition
Feb 2024
Online Event
Home
Process Validation for Biotechnological Products - US edition
Key Topics
Process Qualification (DS & DP)
Process Design (DS & DP)
Ancillary Process Validation Studies
Continued Process Verification (DS & DP)
Who should Attend
CMC development program managers
Process development scientists and managers
Manufacturing managers
Pharmaceutical development scientists and managers
Heads of Quality Assurance
QC and stability control managers
Drug Regulatory Affairs managers
Read more
Past Events
Process Validation for Biotechnological Products - US edition - Feb 2024, Online Event
(98205)
Process Validation for Biotechnological Products - EU edition - 2024, Online Event
(95171)
Process Validation for Biotechnological Products - Clinical Project Management - US edition - 13-16 Feb 2023, Online Event
(98204)
Process Validation for Biotechnological Products - EU edition - 07-08 Feb 2023, Online Event
(92575)
Process Validation for Biotechnological Products - US 2026
Important
Please, check "Process Validation for Biotechnological Products - US" official website for possible changes, before making any traveling arrangements
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Health & Medicine:
Pharma
Technology:
Biotechnology
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