Search results for " review"
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				Operational Excellence: More Than Just Process Improvement
								Compliance specialists were created to rotate through the operations area and to spend 80% of their time on the shop floor to provide real-time, in-process batch record documentation review and mentor…								
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				Essentials in Quality Risk Management
								  
	
	
	
	
	
	
	
	Risk communication and review
	
	Once the risk assessment and the control actions have been determined, it is crucial in the QRM process to communicate the actions to p…								
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				QbD and PAT in Upstream and Downstream Processing
								The risk assessment includes a review and assessment of the products CQAs when manufactured on specific equipment. 
	
	BioPharm: In implementing QbD, what would you identify as the critical process …								
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				PDA's Technical Report for Biotech Cleaning Validation
								49 include change control, risk-based periodic monitoring, and data trending review. Training and retraining for manual cleaning processes are also significant because they are the primary mechanisms …								
								 
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				How To Execute Successful Data Migrations
								Assign experienced QA resources to review and test business and technical requirements. 
			
			
				Have QA resources work in tandem with business analysts to review detailed transformation/mapping s…								
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				Reimagining Affordable Biosimilars
								A review of biosimilars approved in the past five years suggests increasing use of rodents followed by NHPs for PK studies and mice for PD studies (25) (see Table II). When the target antigen of the b…								
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				Good Manufacturing Practices: Challenges with Compliance
								Do a thorough review, not only of the requirements set out by FDA and other regulatory bodies, but also the World Health Organization’s comprehensive set of annexes related to biological products.
	
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				The Importance of Partnering for Bioanalytical Studies
								These involve a lot of experimentation, data curation and storage, quality review, personnel training, generation of SOPs, etc.—all related documentation should be available for review by FDA, along w…								
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				Leveraging Computational Models of Glycosylation for Biopharma QA
								This review focuses on how different modeling strategies can be leveraged to aid in product QA across the different stages of biopharmaceutical product development and manufacture. Technical details o…