answersLogoWhite

0

Example: 30 and 42

Factor them.

2 x 3 x 5 = 30

2 x 3 x 7 = 42

Select the common factors.

2 x 3 = 6, the GCF

User Avatar

Wiki User

10y ago

What else can I help you with?

Related Questions

What is jb of gcp's real name?

Adrian homer


Do triband phones work in America?

It depends you guys is there a GCP in your state.


Is there a need to follow GCP guidelines for phase 1 studies?

yes


Is there need to follow GCP guidelines for phase 1 study?

yes


What does R1 stand for in E6 R1 in ICH GCP guidelines?

Revision1


Per GCP who is responsible for ensuring that the IRB used for study meets regulations?

Sponsor?


Can you use NBSciencecom website for GCP certification and medical conference registration?

Yes, you can use nbscience.com


State of Co unclaimed taxes and where's the list of people who are on this list?

Visit the Colorado State Treasurer's web site: http://www.colorado.gov/treasury/gcp/


Where is KBR office in Dubai?

GCP Building, 4th Floor Dubai Internet City PO Box 120727 Dubai, United Arab Emirates Phone: 971.4.313.7444


What are the answers for GCP ks2 English sat buster the gondrots?

1) we dont know a millionth of one percent about anything a: the writer wrote in the beginning to hook the reader in


What are the ICH GCP guidelines?

ICH-GCP refers to Guideline E6(R1): Good Clinical Practice : Consolidated Guideline, prepared by the International Conference of Harmonisation.It was finalised in May 1996 and describes the responsibilities and expectations of all participants in the conduct of clinical trials, including investigators, monitors, sponsors and IRBs (ethics committees). GCPs cover aspects of monitoring, reporting and archiving of clinical trials, and Essential Documents.


What does E6 stand E6 in ICH GCP guidelines?

E6 refers to the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guideline on Good Clinical Practice (GCP). This guideline sets out the standards for designing, conducting, recording, and reporting clinical trials involving human subjects. It ensures that the rights, safety, and well-being of trial participants are protected, and that the data generated is reliable and credible.