메뉴 건너뛰기




Volumn 61, Issue 7, 1999, Pages 656-661

Drying of pharmaceutical granules in single pot systems;Trocknung pharmazeutischer granulate in eintopfsystemen

Author keywords

[No Author keywords available]

Indexed keywords

DRUG FORMULATION; DRUG GRANULATION; DRY POWDER; METHODOLOGY; PHARMACEUTICAL ENGINEERING; REVIEW; TABLET FORMULATION; TECHNOLOGY;

EID: 0032838734     PISSN: 0031711X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (2)

References (44)
  • 5
    • 0344385656 scopus 로고
    • Preprints, VDI, Düsseldorf
    • "Trocknungstechnik", Preprints, VDI, Düsseldorf (1991)
    • (1991) Trocknungstechnik
  • 16
  • 28
    • 0344817365 scopus 로고    scopus 로고
    • Möglichkeiten der prozeßsteuerung- und überwachung von granulierungs-trocknungs-prozessen
    • Heidelberg
    • List, K., Möglichkeiten der Prozeßsteuerung- und Überwachung von Granulierungs-Trocknungs-Prozessen, Vortrag Concept-Seminar "Stand der Technik in der Solida Produktion", Heidelberg (1996)
    • (1996) Vortrag Concept-Seminar "Stand der Technik in der Solida Produktion"
    • List, K.1
  • 38
    • 0345680143 scopus 로고
    • Demonstration-microwave/vacuum drying of pharmaceuticals
    • Washington DC
    • Moss, R. A., Demonstration-Microwave/vacuum Drying of Pharmaceuticals, AAPS Annual Meeting, Washington DC (1991)
    • (1991) AAPS Annual Meeting
    • Moss, R.A.1
  • 39
    • 0344817357 scopus 로고
    • Microwave vacuum processing in the Vactron 300
    • Washington DC
    • van Scoik, K., Microwave Vacuum Processing in the Vactron 300, AAPS Annual Meeting, Washington DC (1991)
    • (1991) AAPS Annual Meeting
    • Van Scoik, K.1
  • 43
    • 0009302055 scopus 로고    scopus 로고
    • Immedeate release solid oral dosage forms; scale-up and postapproval changes: Chemistry, manufacturing, and controls; in vitro dissolution testing; in vivo bioequivalence documentation; guidance
    • FDA, Immedeate release solid oral dosage forms; scale-up and postapproval changes: chemistry, manufacturing, and controls; in vitro dissolution testing; in vivo bioequivalence documentation; guidance, Fed. Reg. 60, 61638
    • Fed. Reg. , vol.60 , pp. 61638


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.