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PharmTech
2 天
Regulatory Authority Actions
CDER Director Patrizia Cavazzoni and CBER Director Peter Marks provided an update on the rare disease innovation hub in a new FDA Voices blog post.
PharmTech
9 天
Behind the Headlines: What the U.S. Election Results Mean for Industry, In Vivo CAR-T ...
Brian Feth and Jonathan Grinstein go behind the headlines to discuss the impact of a Republican administration on Federal ...
PharmTech
12 天
AAPS PharmSci 360: Challenges in Peptide-Based Drugs
Pharmaceutical Technology® caught up with Brittany Hayes, PhD, Highly Potent & Oncology Platform Director at CordenPharma, ...
PharmTech
2 天
Peter Langguth
Application of Validation Principles to the Training Quality System: Part 9, Quality Risk Management Hazard Identification ...
PharmTech
2 天
Stephanie Snow
Application of Validation Principles to the Training Quality System: Part 9, Quality Risk Management Hazard Identification ...
PharmTech
2 天
Martin Koeberle
Application of Validation Principles to the Training Quality System: Part 9, Quality Risk Management Hazard Identification ...
PharmTech
2 天
Imjak Jeon
Application of Validation Principles to the Training Quality System: Part 9, Quality Risk Management Hazard Identification ...
PharmTech
2 天
Hellen Berger
Application of Validation Principles to the Training Quality System: Part 9, Quality Risk Management Hazard Identification ...
PharmTech
2 天
Johan Remmelgas
Application of Validation Principles to the Training Quality System: Part 9, Quality Risk Management Hazard Identification ...
PharmTech
2 天
Antonio Moroni, PhD
Application of Validation Principles to the Training Quality System: Part 9, Quality Risk Management Hazard Identification ...
PharmTech
2 天
Kate Coleman
Application of Validation Principles to the Training Quality System: Part 9, Quality Risk Management Hazard Identification ...
PharmTech
3 天
Improving Content Uniformity of Morphologically Challenging APIs by Excipient Choice
Traditional formulations commonly struggle to achieve content uniformity with morphologically challenging active pharmaceutical ingredients (APIs), requiring the use of complicated processes such as ...
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