Terminology
Data and Documents
Agencies
Biology
Trials
100

is a combination of multiple fields of science used to benefit the study of life.

Biotechnology

100

This document shows personnel how to carry out a process

SOP or standard Operating Procedures

100

What government agency is responsible for overlooking GMOs in a general sense

FDA 

100

This terminology refers to the approach to life science research. 

Systems Biology

100

This stage of clinical trials is used to determine dosage of medication

Stage I

200
This word is used for the tests that are conducted in a laboratory

Assay

200

This is a way of protecting investors and companies for developing a new product

Patent

200

Testing Modified Plants in the field is covered by what government agency?

APHIS

200

 investigates the entire genome, the entirety of DNA in the cell.

Genomics

200

This stage of clinical trials is the first stage where affected individuals are tested on. It is typically a small group of individuals. 

Stage II

300

Before a drug can be sold to the public, it must go through these stages of testing

Clinical Trials

300

This is the most professional way of presenting data. It occurs between scientists

Peer-Review Publications

300

APHIS is a subcategory of what federal agency?

USDA

300

studies the entire protein complement of a cell or organism.

Proteomics

300
This stage of trials is tested on a small group of healthy individuals

Stage I

400

These guidelines assure proper design, monitoring, and control of manufacturing processes and facilities.

cGMP or Current Good Manufacturing Practices

400

This way of presenting information is less formal and occurs to an audience of the general population.

Seminars, conferences, Meetings

400

What government agency is responsible for monitoring the culturing of genetically modified organisms?

EPA

400

investigates the metabolites in a cell or organism.

Metabolomics

400

Which stage of trial is used to detect side effects 

Stage III

500

 This ensures sound laboratory procedures are being followed. Companies must fulfill required paperwork and documentation.

cGLP or Current Good Laboratory Practices

500

This document is used by the QC and Manufacturing department which contains the data for a product being created

Batch Record

500

studies the RNA transcript that is expressed.

Transcriptomics

500

This stage of clinical trials is tested on a large group of affected individuals

Stage III

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