Radiopharmaceuticals: Drug Development and Regulatory Issues
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-540-76735-0_20.pdf
Reference28 articles.
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2. Barrio JR, Marcus CS, Hung JC, et al (2004) A rational regulatory approach for positron emission tomography imaging probes: from “first in man” to NDA approval and reimbursement. Mol Imag Biol 6:361–367
3. Bergstrom M, Grahnen A, Langstrom B (2003) Positron emission tomography micro dosing: a new concept with application in tracer and early clinical drug development. Eur J Clin Pharmacol 59(5–6):357–366
4. Callahan RJ, Chilton HM, Ponto JA, et al (2007) Procedure guideline for the use of radiopharmaceuticals 4.0. J Nucl Med Tech 35(4):272–275
5. Eckelman WC, Rohatagi S, Krohn KA, et al (2005) Are there lessons to be learned from drug development that will accelerate the use of molecular imaging probes in the clinic? Nucl Med Biol 32(7):657–662
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