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

Journal of chromatographic science, 2008-07, Vol.46 (6), p.461-465

2008

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

Chromatographia, 2009-02, Vol.69 (3-4), p.187-194

2009

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Early Development GMPs for stability: an industry perspective (Part IV)

Pharmaceutical technology Europe, 2012-10, Vol.24 (10), p.61

2012

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Addition of azides to C60 : synthesis of azafulleroids

Journal of the American Chemical Society, 1993-02, Vol.115 (3), p.1148-1150

1993

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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

Journal of pharmaceutical innovation, 2012-12, Vol.7 (3-4), p.214-224

2012

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

Journal of chromatographic science, 1998-03, Vol.36 (3), p.119-124

1998

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Electrochemical Evidence for Through-Space Orbital Interactions in Spiromethanofullerenes

Angewandte Chemie (International ed.), 1995-08, Vol.34 (15), p.1591-1594

1995

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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

Journal of pharmaceutical innovation, 2013-03, Vol.8 (1), p.56-65

2013

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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

Journal of pharmaceutical innovation, 2013-12, Vol.8 (4), p.229-239

2013

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

Journal of the American Chemical Society, 1992-12, Vol.114 (26), p.10656-10657

1992

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

Journal of chromatographic science, 2000-06, Vol.38 (6), p.246-254

2000

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

Pharmaceutical Technology, 2014-12, Vol.38 (12), p.38

2014

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

Pharmaceutical Technology, 2014-11, Vol.38 (11), p.48

2014

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Elektrochemischer Nachweis von "Through-space"-Wechselwirkungen in Spiromethanofullerenen

Angewandte Chemie, 1995-08, Vol.107 (15), p.1733-1735

1995

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Addition of azides to fullerene C60: synthesis of azafulleroids

Journal of the American Chemical Society, 1993-02, Vol.115 (3), p.1148-1150

1993

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Elektrochemischer Nachweis von “Through‐space”‐Wechselwirkungen in Spiromethanofullerenen

Angewandte Chemie, 1995-08, Vol.107 (15), p.1733-1735

1995

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

Journal of chromatographic science, 1998, Vol.36 (3), p.119-124

1998

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

Journal of the American Chemical Society, 1992, Vol.114 (26), p.10656-10657

1992

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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

Pharmaceutical technology (2003), 2014-12, Vol.38 (12), p.38

2014

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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

Pharmaceutical technology (2003), 2014-11, Vol.38 (11), p.48

2014

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

Pharmaceutical technology (2003), 2012-09, Vol.36 (9), p.64

2012

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Promising High-Confinement Regime for Steady-State Fusion

Physical review letters, 2019-06, Vol.122 (25), p.255001-255001, Article 255001

2019

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

The Lancet (British edition), 2003-10, Vol.362 (9393), p.1353-1358

2003

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Short- and potential long-term adverse health outcomes of COVID-19: a rapid review

Emerging microbes & infections, 2020-01, Vol.9 (1), p.2190-2199

2020

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Integrating postradiotherapy plasma Epstein–Barr virus DNA and TNM stage for risk stratification of nasopharyngeal carcinoma to adjuvant therapy

Annals of oncology, 2020-06, Vol.31 (6), p.769-779

2020

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

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

Early Development GMPs for stability: an industry perspective (Part IV)

Addition of azides to C60 : synthesis of azafulleroids

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

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

Electrochemical Evidence for Through-Space Orbital Interactions in Spiromethanofullerenes

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

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

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

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

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

Elektrochemischer Nachweis von "Through-space"-Wechselwirkungen in Spiromethanofullerenen

Addition of azides to fullerene C60: synthesis of azafulleroids

Elektrochemischer Nachweis von “Through‐space”‐Wechselwirkungen in Spiromethanofullerenen

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

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

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

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

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

Promising High-Confinement Regime for Steady-State Fusion

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

Short- and potential long-term adverse health outcomes of COVID-19: a rapid review

Integrating postradiotherapy plasma Epstein–Barr virus DNA and TNM stage for risk stratification of nasopharyngeal carcinoma to adjuvant therapy

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