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Definitions from the Web

Term: Ich Guidelines Clinical Research

Definition:

The Ich Guidelines Clinical Research refers to the set of guidelines provided by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) specifically designed for the conduct of clinical trials and research in the pharmaceutical industry.

Senses and Usages:

Sense 1 (noun):

Ich Guidelines Clinical Research comprehensively outline the industry-accepted standards and practices for designing, conducting, recording, and reporting clinical trials and research in the pharmaceutical field.

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Sense 2 (adjective - popular):

Ich Guidelines Clinical Research popularly refers to the widely recognized and adopted principles and protocols followed by pharmaceutical companies during the different stages of clinical trials and research.

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Sense 3 (adjective - local):

In the local context, Ich Guidelines Clinical Research pertains to the specific adaptations and interpretations of the international guidelines made by regulatory bodies at the national or local level.

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Sample Sentences:

1. The implementation of Ich Guidelines Clinical Research ensures that clinical trials are conducted with ethical standards and scientific rigor.
2. Researchers must adhere to the Ich Guidelines Clinical Research when designing clinical protocols for new drug development.
3. Learning about the Ich Guidelines Clinical Research is crucial for individuals pursuing a career in the pharmaceutical industry.
4. Local regulatory authorities endorse the adoption of Ich Guidelines Clinical Research as a basis for the approval and monitoring of clinical trials within their jurisdiction.