William Wang – författare
Visar alla böcker från författaren William Wang. Handla med fri frakt och snabb leverans.
11 produkter
Simultaneous Global New Drug Development
Multi-Regional Clinical Trials after ICH E17
Av Gang Li, Bruce Binkowitz m. fl.
Inbunden, 2021
2828 kr
Lägg i varukorg
Global simultaneous development is becoming more necessary as the cost of developing medical products continues to grow. The strategy of using multiregional clinical trials (MRCTs) has become the preferred method for developing new medicines. Implementing the same protocol to include subjects from …
Simultaneous Global New Drug Development
Multi-Regional Clinical Trials after ICH E17
Av Gang Li, Bruce Binkowitz m. fl.
Häftad, 2024
1252 kr
Lägg i varukorg
Global simultaneous development is becoming more necessary as the cost of developing medical products continues to grow. The strategy of using multiregional clinical trials (MRCTs) has become the preferred method for developing new medicines. Implementing the same protocol to include subjects from …
Quantitative Drug Safety and Benefit Risk Evaluation
Practical and Cross-Disciplinary Approaches
Av Judy Li, James Buchanan m. fl.
E-bok, 2021
1034 kr
Lägg i varukorg
Quantitative Methodologies and Process for Safety Monitoring and Ongoing Benefit Risk Evaluation provides a comprehensive coverage on safety monitoring methodologies, covering both global trends and regional initiatives. Pharmacovigilance has traditionally focused on the handling of individual …
Quantitative Drug Safety and Benefit Risk Evaluation
Practical and Cross-Disciplinary Approaches
Av Judy Li, James Buchanan m. fl.
E-bok, 2021
1034 kr
Lägg i varukorg
Quantitative Methodologies and Process for Safety Monitoring and Ongoing Benefit Risk Evaluation provides a comprehensive coverage on safety monitoring methodologies, covering both global trends and regional initiatives. Pharmacovigilance has traditionally focused on the handling of individual …
Simultaneous Global New Drug Development
Multi-Regional Clinical Trials after ICH E17
E-bok, 2021
1320 kr
Lägg i varukorg
Global simultaneous development is becoming more necessary as the cost of developing medical products continues to grow. The strategy of using multiregional clinical trials (MRCTs) has become the preferred method for developing new medicines. Implementing the same protocol to include subjects from …
Simultaneous Global New Drug Development
Multi-Regional Clinical Trials after ICH E17
E-bok, 2021
1320 kr
Lägg i varukorg
Global simultaneous development is becoming more necessary as the cost of developing medical products continues to grow. The strategy of using multiregional clinical trials (MRCTs) has become the preferred method for developing new medicines. Implementing the same protocol to include subjects from …
Quantitative Drug Safety and Benefit Risk Evaluation
Practical and Cross-Disciplinary Approaches
Av William Wang, Melvin Munsaka m. fl.
Häftad, 2024
877 kr
Lägg i varukorg
Quantitative Methodologies and Process for Safety Monitoring and Ongoing Benefit Risk Evaluation provides a comprehensive coverage on safety monitoring methodologies, covering both global trends and regional initiatives. Pharmacovigilance has traditionally focused on the handling of individual …
Master Protocol Clinical Trials for Evidence Generation
Strategies, Designs, Operations, and Case Studies
Av Ruixiao Lu, Jingjing Ye m. fl.
Inbunden, 2026
2198 kr
Lägg i varukorg
Drug development is at a crossroads. As personalized medicine and targeted therapies expand, traditional clinical trial models have become too slow, costly, and inefficient. To meet the urgent need for faster, reliable evidence generation and decision making, researchers and regulators alike have …
Master Protocol Clinical Trials for Evidence Generation
Strategies, Designs, Operations, and Case Studies
Av William Wang, Chengxing (Cindy) Lu m. fl.
E-bok, 2026
960 kr
Lägg i varukorg
Drug development is at a crossroads. As personalized medicine and targeted therapies expand, traditional clinical trial models have become too slow, costly, and inefficient. To meet the urgent need for faster, reliable evidence generation and decision making, researchers and regulators alike have …
Master Protocol Clinical Trials for Evidence Generation
Strategies, Designs, Operations, and Case Studies
Av William Wang, Chengxing (Cindy) Lu m. fl.
E-bok, 2026
981 kr
Lägg i varukorg
Drug development is at a crossroads. As personalized medicine and targeted therapies expand, traditional clinical trial models have become too slow, costly, and inefficient. To meet the urgent need for faster, reliable evidence generation and decision making, researchers and regulators alike have …
Quantitative Drug Safety and Benefit Risk Evaluation
Practical and Cross-Disciplinary Approaches
Av William Wang, Melvin Munsaka m. fl.
Inbunden, 2021
2588 kr
Lägg i varukorg
Quantitative Methodologies and Process for Safety Monitoring and Ongoing Benefit Risk Evaluation provides a comprehensive coverage on safety monitoring methodologies, covering both global trends and regional initiatives. Pharmacovigilance has traditionally focused on the handling of individual …
