DUBLIN–(BUSINESS WIRE)–Apr 26, 2018–The “Applied Statistics for FDA Process Validation” conference has been added to ResearchAndMarkets.com’s offering.
Course “Applied Statistics for FDA Process Validation” has been pre-approved by RAPS as eligible for up to 12 credits towards a participant’s RAC recertification upon full completion.
Stage 1: Process Design: The commercial manufacturing process is defined during this stage based on knowledge gained through development and scale-up activities.
Stage 2: Process Qualification: During this stage, the process design is evaluated to determine if the process is capable of reproducible commercial manufacturing.
Stage 3: Continued Process Verification: Ongoing assurance is gained during routine production that the process remains in a state of control.
Who Will Benefit:
This seminar is designed for pharmaceutical and biopharmaceutical professionals who are involved with product and/or process design, validation, or manufacturing/control.Process Scientist/EngineerDesign EngineerProduct Development EngineerRegulatory/Compliance ProfessionalDesign Controls EngineerSix Sigma Green BeltSix Sigma Black BeltContinuous Improvement Manager
For more information about this conference visit https://ift.tt/2r2Q90S
View source version on businesswire.com:https://ift.tt/2HzEtsL
CONTACT: ResearchAndMarkets.com
Laura Wood, Senior Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
Related Topics:Pharmaceutical Manufacturing
KEYWORD: UNITED STATES NORTH AMERICA PENNSYLVANIA
INDUSTRY KEYWORD: HEALTH BIOTECHNOLOGY PHARMACEUTICAL
SOURCE: Research and Markets
Copyright Business Wire 2018.
PUB: 04/26/2018 06:21 PM/DISC: 04/26/2018 06:21 PM
https://ift.tt/2r0Dv2s
Copyright Business Wire 2018.
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