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The Precision Blog
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Read Case Study: Conducting Autologous Cell Therapy Research Across 3 Continents with Zero Sample Loss
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Read Key Strategies for Future-Proofing Gene Therapy Assays Key Strategies for Future-Proofing Gene Therapy Assays
Read Phase 1 Clinical Trial Designs Explained: BOIN, CRM, BLRM & Modern Adaptive Strategies Phase 1 Clinical Trial Designs Explained: BOIN, CRM, BLRM & Modern Adaptive Strategies
Read Empowering Clinical Operations with Enhanced Biospecimen Lifecycle Management Empowering Clinical Operations with Enhanced Biospecimen Lifecycle Management
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Read: Case Study: Conducting Autologous Cell Therapy Research Across 3 Continents with Zero Sample Loss 
Case Study: Conducting Autologous Cell Therapy Research Across 3 Continents with Zero Sample Loss
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Read: Phase 1 Clinical Trial Designs Explained: BOIN, CRM, BLRM & Modern Adaptive Strategies 
Phase 1 Clinical Trial Designs Explained: BOIN, CRM, BLRM & Modern Adaptive Strategies
has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778891, hs_child_table_id=0, hs_updated_at=1709645745122, hs_published_at=1748379090824, description=Kurt Preugschat has over 11 years of statistical experience from Phase I to Phase IV clinical trials. He is a lead statistician, providing statistical support and oversight for numerous clinical trials associated with new drug applications (NDA), supplemental new drug applications (sNDA), and medical devices. His expertise includes the development of study designs to meet complex clinical questions and the measurement of desired outcomes. In addition, Kurt has extensive experience generating statistical analyses and creating complex SAS programs and macros used by study team., avatar=Image{width=150,height=150,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/PfMxMarkentive/authors/kurt-preugschat.webp',altText='',fileId=null}, linkedin=https://www.linkedin.com/in/kurt-preugschat-97298923a, hs_name=, hs_path=, lastname=Preugschat, hs_initial_published_at=1716136551646, hs_created_at=1709645745122, hs_is_edited=false, hs_deleted_at=0, name=Kurt, job=, slug=kurt-preugschat, email=, hs_updated_by_user_id=51739740}, second={}, third={}}) -
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Read: Phase I Clinical Trial Designs: Continuous Reassessment Method (CRM) 
Phase I Clinical Trial Designs: Continuous Reassessment Method (CRM)
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Read: Key Strategies for Future-Proofing Gene Therapy Assays 
Key Strategies for Future-Proofing Gene Therapy Assays
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Read: Gene Therapy Assays: Regulatory Compliance with Unified Immunogenicity 
Gene Therapy Assays: Regulatory Compliance with Unified Immunogenicity
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Read: Optimizing Immunohistochemistry Validation and Regulatory Strategies 
Optimizing Immunohistochemistry Validation and Regulatory Strategies
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All articles
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Read: COVID-19 Home Testing: Looking Back at the Journey to Authorization 
COVID-19 Home Testing: Looking Back at the Journey to Authorization
has not third author: true, (SizeLimitingPyMap: {main={hs_id=159488778851, hs_child_table_id=0, hs_updated_at=1715692769174, hs_published_at=1748379090824, description=Jo-ann Fabia Gonzales is an experienced regulatory affair professional with more than 20 years of experience in biotechnology. Her career has a rich focus on medical devices and IVD regulatory support., avatar=Image{width=720,height=896,url='https://5014803.fs1.hubspotusercontent-na1.net/hubfs/5014803/PfM%20Website/Headshots/Headshots%20no%20background/Joann_Gonzales.png',altText='Joann_Gonzales',fileId=167372995923}, linkedin=https://www.linkedin.com/in/joannfabilagonzales-57527a4, hs_name=, hs_path=, lastname=Fabia Gonzales, hs_initial_published_at=1716212769184, hs_created_at=1709645745082, hs_is_edited=false, hs_deleted_at=0, name=Jo-ann, job=, slug=jo-ann-fabia-gonzales, email=, hs_updated_by_user_id=51739740}, second={}, third={}}) -
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Read: IVD Manufacturers & EU IVD Regulation Changes (May 2022) 
IVD Manufacturers & EU IVD Regulation Changes (May 2022)
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