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The FDAzilla family of products unlocks regulatory insights and reduces risk for FDA regulated businesses. Expert Guidance from Barb Unger. Read the Medical Device Blog. Week of Mar 4th 2018 FDA Sent These Warning Letters to Pharma Companies. CGMP Quality Assurance and FDA 483s. 74 New FDA 483s March 15th 2018.
No sentido de ajudar no desempenho, demonstração e manutenção do estado de certificação das Boas Práticas. Através de artigos com abordagens estratégicas, comentários, tópicos de treinamentos, ferramentas e estudos de caso. Assim como informações sobre a conduta e desenvolvimento das pessoas envolvidas neste segmento. Sexta-feira, 27 de fevereiro de 2015.
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This blog is straight talk about quality assurance in the pharmaceutical industry. Not the technical aspects as much as the challenges faced by company management and their internal quality assurance professionalssometimes side-by-side and often toe-to-toe. Saturday, March 28, 2015. 12 Ways to Improve Procedures. Procedures are often more form than function. Words on a page do not necessarily make things happen as intended. I have observed the general neglect of procedures for many years and hav.Witho.CONTENT
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