Reference no: EM132998234 , Length: word count:400

Discussion: Regulatory Compliance

Introduction
As a clinical research coordinator, you will need to know if your study has received all of the approvals, all the documents have been signed, and that your clinical trial is cleared to enroll patients.

Instructions

1. In your initial post, in your own words, define regulatory compliance.

2. Respond to one classmate and describe two challenges and two opportunities for regulatory compliance.

3. Respond to a different classmate's challenge and explain how you would overcome one challenge they have listed.

Submission

In response to each topic or prompt provided by the instructor, please do the following:

1. Provide a thoughtful and complete initial post that is two to three paragraphs (minimum of 400 words) by the instructor's due date.

2. Provide a two to three paragraph response (minimum 400 words), to two or more classmates that directly addresses your thoughts on their post.

3. In your post or response, reference either material in the book or an external source to support your point. Don't forget to cite your source.

4. Please ensure that each response includes proper grammar and punctuation and is respectful in tone.

Attachment:- Discussion- Regulatory Compliance.rar