Regulatory considerations in production of a cell therapy medicinal product in Europe to clinical research.
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Stem cell bioprocess engineering towards cGMP production and clinical applicationsClinical research skills development program in cell-based regenerative medicine.Standard requirement of a microbiological quality control program for the manufacture of human mesenchymal stem cells for clinical use.[Advanced medicinal products medical therapy based on mesenchymal stem cells].
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Regulatory considerations in production of a cell therapy medicinal product in Europe to clinical research.
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Regulatory considerations in p ...... n Europe to clinical research.
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Regulatory considerations in p ...... n Europe to clinical research.
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Regulatory considerations in p ...... n Europe to clinical research.
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P2093
P2860
P1476
Regulatory considerations in p ...... n Europe to clinical research.
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P2093
Adolfina Ruiz Martinez
Beatriz Clares Naveros
Patricia Gálvez Martín
Visitación Gallardo Lara
P2860
P2888
P356
10.1007/S10238-012-0213-6
P577
2012-09-27T00:00:00Z
P5875
P6179
1014276604