Martin-Moe S[au] - Search Results

Year	Number of Results
1995	1
2000	1
2004	1
2007	1
2008	1
2010	1
2011	1
2024	0

1

On developing a process for conducting extractable-leachable assessment of components used for storage of biopharmaceuticals.

Wakankar AA, Wang YJ, Canova-Davis E, Ma S, Schmalzing D, Grieco J, Milby T, Reynolds T, Mazzarella K, Hoff E, Gomez S, Martin-Moe S. Wakankar AA, et al. Among authors: martin moe s. J Pharm Sci. 2010 May;99(5):2209-18. doi: 10.1002/jps.22012. J Pharm Sci. 2010. PMID: 20039383 Review.

2

Oxidation of protein by vaporized sanitizing agents.

Wang W, Cui TY, Wang YJ, Martin-Moe S. Wang W, et al. Among authors: martin moe s. PDA J Pharm Sci Technol. 2004 May-Jun;58(3):121-9. PDA J Pharm Sci Technol. 2004. PMID: 15233252

3

Stabilization of a polypeptide in non-aqueous solvents.

Wang W, Martin-Moe S, Pan C, Musza L, Wang YJ. Wang W, et al. Among authors: martin moe s. Int J Pharm. 2008 Mar 3;351(1-2):1-7. doi: 10.1016/j.ijpharm.2007.09.012. Epub 2007 Sep 15. Int J Pharm. 2008. PMID: 17964744

4

A new roadmap for biopharmaceutical drug product development: Integrating development, validation, and quality by design.

Martin-Moe S, Lim FJ, Wong RL, Sreedhara A, Sundaram J, Sane SU. Martin-Moe S, et al. J Pharm Sci. 2011 Aug;100(8):3031-3043. doi: 10.1002/jps.22545. Epub 2011 Mar 18. J Pharm Sci. 2011. PMID: 21425164

5

Validation of critical process input parameters in the production of protein pharmaceutical products: a strategy for validating new processes or revalidating existing processes.

Martin-Moe S, Ellis J, Coan M, Victor R, Savage J, Bogren N, Leng B, Lee C, Burnett M, Montgomery P. Martin-Moe S, et al. PDA J Pharm Sci Technol. 2000 Jul-Aug;54(4):315-9. PDA J Pharm Sci Technol. 2000. PMID: 10969528 No abstract available.

6

Hydrophobic interactions and the design of receptor mimetic peptides.

Martin-Moe SA, Lehr R, Cauley MD, Moe GR. Martin-Moe SA, et al. Pept Res. 1995 Mar-Apr;8(2):70-6. Pept Res. 1995. PMID: 7544657

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