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- W66052945 abstract "The development of efficient lentivectors brings about exciting possibilities for novel therapeutic interventions. Still, as new biologicals intended to be used in the clinic, these vectors will have to comply with a complete set of requirements regarding their mode of preparation and characterization. Over the past 50 years, there has been an increasing awareness of the safety issues surrounding the manufacturing of medicinal products. Regulatory authorities and agencies regularly publish guidelines and coordinate international conferences on harmonization (ICH), whose goal is to define common standards for biotechnological and biological products to be administered to human patients (SCHULTZ 1998)." @default.
- W66052945 created "2016-06-24" @default.
- W66052945 creator A5031915986 @default.
- W66052945 creator A5043124146 @default.
- W66052945 creator A5062324391 @default.
- W66052945 date "2002-01-01" @default.
- W66052945 modified "2023-10-18" @default.
- W66052945 title "Biosafety Issues in Lentivector Production" @default.
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