Search Results - CHAN LI, Q

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  1. 1
    HPLC-UV Method Development and Validation for the Determination of Low Level Formaldehyde in a Drug Substance

    HPLC-UV Method Development and Validation for the Determination of Low Level Formaldehyde in a Drug Substance by Soman, A., Qiu, Y., Chan Li, Q.

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  2. 2
    A Scientific, General Approach to Robustness Validation for an Ion-Pair LC Assay Method Through a Case Study

    A Scientific, General Approach to Robustness Validation for an Ion-Pair LC Assay Method Through a Case Study by Chan Li, Q., Cohen, Kenneth, Meagan, Paul

    Published in Chromatographia
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  3. 3
    Early Development GMPs for stability: an industry perspective (Part IV)

    Early Development GMPs for stability: an industry perspective (Part IV) by Acken, Bruce, Alasandro, Mark, Colgan, Stephen, Curry, Paul, Diana, Frank, Chan Li, Q, Jane Li, Z, Mazzeo, Tony, Rignall, Andy, Tan, Jessica Z, Timpano, Robert

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  4. 4
    Addition of azides to C60 : synthesis of azafulleroids

    Addition of azides to C60 : synthesis of azafulleroids by PRATO, M, CHAN LI, Q, WUDL, F

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  5. 5
    Best Practices for Drug Substance Stress and Stability Studies During Early-Stage Development Part I—Conducting Drug Substance Solid Stress to Support Phase Ia Clinical Trials

    Best Practices for Drug Substance Stress and Stability Studies During Early-Stage Development Part I—Conducting Drug Substance Solid Stress to Support Phase Ia Clinical Trials by Li, Q. Chan, Qiu, F., Cohen, K., Tougas, T., Li, J., McCaffrey, J., Purdue, T., Song, Jinhua J., Swanek, F., Abelaira, S.

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  6. 6
    A Capillary Gas Chromatographic Procedure for the Analysis of Nine Common Residual Solvents in Water-Insoluble Bulk Pharmaceuticals

    A Capillary Gas Chromatographic Procedure for the Analysis of Nine Common Residual Solvents in Water-Insoluble Bulk Pharmaceuticals by Li, Q. Chan, Cohen, Kenneth A., Zhuang, G.

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  7. 7
    Best Practices for Drug Substance Stress and Stability Studies During Early-Stage Development Part II—Conducting Abbreviated Long-Term and Accelerated Stability Testing on the First Clinical Drug Substance Batch to Confirm and Adjust the Drug Substance Retest Period/Powder for Oral Solution Shelf Life

    Best Practices for Drug Substance Stress and Stability Studies During Early-Stage Development Part II—Conducting Abbreviated Long-Term and Accelerated Stability Testing on the Firs... by Li, Q. Chan, Cohen, K., Tougas, T., Qiu, F., Li, J., McCaffrey, J., Purdue, T., Song, Jinhua J., Swanek, F., Abelaira, S.

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  8. 8
    Best Practices for Drug Substance Stress and Stability Studies During Early Stage Development. Part III—How to Make Science- and Risk-based Stability Testing Decisions for Drug Substance Batches Produced after Manufacturing Process Changes

    Best Practices for Drug Substance Stress and Stability Studies During Early Stage Development. Part III—How to Make Science- and Risk-based Stability Testing Decisions for Drug Sub... by Li, Q. Chan, Qiu, Fenghe, McWilliams, Will, Pape, Cheryl, Song, Jinhua J., Swanek, Frank, Wang, Xiao-jun, Cohen, Kenneth, O’Connor, Dennis

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  9. 9
    A polyester and polyurethane of diphenyl C61: retention of fulleroid properties in a polymer

    A polyester and polyurethane of diphenyl C61: retention of fulleroid properties in a polymer by Shi, S., Khemani, K. C., Li, Q., Wudl, F.

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  10. 10
    Validation of a High-Performance Liquid Chromatography Method for the Assay of and Determination of Related Organic Impurities in Nevirapine Drug Substance

    Validation of a High-Performance Liquid Chromatography Method for the Assay of and Determination of Related Organic Impurities in Nevirapine Drug Substance by Li, Q. Chan, Tougas, T., Cohen, K., Lee, R., Meagan, P., Corson, M., Muchnick, T.

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  11. 11
    Part VII: GMPs fdfc Small-Molecule Drugs in Early DevelopmentWorkshop Summary

    Part VII: GMPs fdfc Small-Molecule Drugs in Early DevelopmentWorkshop Summary by Li, Q Chan, Pellet, Jackson D, Szulc, Michael, Trone, Mark D, Wong-Moon, Kirby

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  12. 12
    GMPs for Small-Molecule Drugs in Early Development: Workshop Summary-Part VI

    GMPs for Small-Molecule Drugs in Early Development: Workshop Summary-Part VI by Li, Q Chan, Pellett, Jackson D, Szulc, Michael, Trone, Mark D, Wong-Moon, Kirby

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  13. 13
    Addition of azides to fullerene C60: synthesis of azafulleroids

    Addition of azides to fullerene C60: synthesis of azafulleroids by Prato, M, Li, Q. Chan, Wudl, F, Lucchini, V

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  14. 14
    A capillary gas chromatographic procedure for the analysis of nine common residual solvents in water-insoluble bulk pharmaceuticals: Drugs and pharmaceuticals

    A capillary gas chromatographic procedure for the analysis of nine common residual solvents in water-insoluble bulk pharmaceuticals: Drugs and pharmaceuticals by CHAN LI, Q, COHEN, K. A, ZHUANG, G

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  15. 15
    A polyester and polyurethane of diphenyl C61 : retention of fulleroid properties in a polymers

    A polyester and polyurethane of diphenyl C61 : retention of fulleroid properties in a polymers by SHI, S, KHEMANI, K. C, CHAN LI, Q, WUDL, F

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  16. 16
    Part VII: GMPs for small-molecule drugs in early development--workshop summary: the authors explore and define common industry approaches and practices when applying GMPs in early development

    Part VII: GMPs for small-molecule drugs in early development--workshop summary: the authors explore and define common industry approaches and practices when applying GMPs in early... by Li, Q. Chan, Pellett, Jackson D, Szulc, Michael, Trone, Mark D, Wong-Moon, Kirby

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  17. 17
    GMPs for small-molecule drugs in early development: workshop summary--Part VI: the authors explore and define common industry approaches and practices when applying GMPs in early development

    GMPs for small-molecule drugs in early development: workshop summary--Part VI: the authors explore and define common industry approaches and practices when applying GMPs in early d... by Li, Q. Chan, Pellett, Jackson D, Szulc, Michael, Trone, Mark D, Wong-Moon, Kirby

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  18. 18
    Early development GMPs for stability: an industry perspective (Part IV)

    Early development GMPs for stability: an industry perspective (Part IV) by Acken, Bruce, Alasandro, Mark, Colgan, Stephen, Curry, Paul, Diana, Frank, Li, Q. Chan, Li, Z. Jane, Mazzeo, Tony, Rignall, Andy, Tan, Z. Jessica, Timpano, Robert

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  19. 19
    Promising High-Confinement Regime for Steady-State Fusion

    Promising High-Confinement Regime for Steady-State Fusion by Xu, G S, Yang, Q Q, Yan, N, Wang, Y F, Xu, X Q, Guo, H Y, Maingi, R, Wang, L, Qian, J P, Gong, X Z, Chan, V S, Zhang, T, Zang, Q, Li, Y Y, Zhang, L, Hu, G H, Wan, B N

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  20. 20
    Epidemiology and cause of severe acute respiratory syndrome (SARS) in Guangdong, People's Republic of China, in February, 2003

    Epidemiology and cause of severe acute respiratory syndrome (SARS) in Guangdong, People's Republic of China, in February, 2003 by Zhong, NS, Zheng, BJ, Li, YM, Poon, LLM, Xie, ZH, Chan, KH, Li, PH, Tan, SY, Chang, Q, Xie, JP, Liu, XQ, Xu, J, Li, DX, Yuen, KY, Peiris, JSM, Guan, Y

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