You will get a thorough review of USP 800 required regulatory documents
Project details
Capitalizing on my experience in the health system pharmacy industry, I will review current versions of USP 800 related documents and guidance. I will discuss your facility's needs and wants as well as concerns or deficiencies of current documents. Then I will perform a systematic review of any existing documents and propose revisions to structure and content to enhance USP compliance and increase usability and transparency. This includes review and discussion of any policies or practices referenced in documents and if necessary recommendations on alternative practices or strategies to achieve compliance. Your suggestions and feedback will be taken into account and further drafts provided as needed. At the end, I will deliver the expected documents in the file format of the client's choice.
What's included
| Service Tiers |
Starter
$50
|
Standard
$100
|
Advanced
$300
|
|---|---|---|---|
| Delivery Time | 7 days | 14 days | 30 days |
Number of Revisions | 1 | 2 | Unlimited |
About Kathryn
Pharmacy Tech specializing in hazardous sterile compounding (USP 800)
Lexington, United States - 6:10 pm local time
Steps for completing your project
After purchasing the project, send requirements so Kathryn can start the project.
Delivery time starts when Kathryn receives requirements from you.
Kathryn works on your project following the steps below.
Revisions may occur after the delivery date.
Discuss current documents and any concerns or requests
Systematic review of current documents and proposal of new drafts