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Volumn 670, Issue , 2010, Pages 31-37

Regulatory considerations in application of encapsulated cell therapies

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CELL ENCAPSULATION; CELL THERAPY; DOCUMENTATION; FOOD AND DRUG ADMINISTRATION; GENE THERAPY; GOOD CLINICAL PRACTICE; GOOD MANUFACTURING PRACTICE; LAW; PRACTICE GUIDELINE; PRIORITY JOURNAL; QUALITY CONTROL; TISSUE ENGINEERING; TISSUE TRANSPLANTATION; TOTAL QUALITY MANAGEMENT; CELL TRANSPLANTATION; CLINICAL TRIAL; DRUG FORMULATION; DRUG INDUSTRY; HUMAN; INSTRUMENTATION; LEGAL ASPECT; METHODOLOGY; REVIEW; UNITED STATES;

EID: 77951626822     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4419-5786-3_4     Document Type: Article
Times cited : (2)

References (10)
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  • 3
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    • De Vos, P.1    Faas, M.M.2    Strand, B.3    Calafiore, R.4
  • 5
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    • Immel BK. A brief history of the GMP's: The power of storytelling. BioPharm International 2000; 61:26-36.
    • (2000) BioPharm International , vol.61 , pp. 26-36
    • Immel, B.K.1
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    • The new GMP environment for investigational medicinal products in the european union
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    • Möritz, A.1
  • 8
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    • Regulatory affairs; If you didn't write it down, it didn't happen. 2006
    • Rosin LJ. Regulatory affairs; If you didn't write it down, it didn't happen. 2006. BioProcess Int Supplement 2006; 4(3):16-23.
    • (2006) BioProcess Int Supplement , vol.4 , Issue.3 , pp. 16-23
    • Rosin, L.J.1
  • 9
    • 79959606979 scopus 로고    scopus 로고
    • Guidance for Industry; Source Animal, product, preclinical and clinical issues regarding the use of xenotransplantation products in humans
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    • (2003)
  • 10
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    • Current and future frameworks for cell- and tissue- based products
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    • Mingam, I.1    Dupraz-Poiseau, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.