Table of Contents
What does PCCA stand for?
PCCA
| Acronym | Definition |
|---|---|
| PCCA | Principal Chief Controller of Accounts |
| PCCA | Portable Computer and Communications Association |
| PCCA | Propionyl-CoA Carboxylase, Alpha Subunit |
| PCCA | Professional Compounding Centers of America, Inc. (pharmacists) |
What does PCCA stand for compounding?
Professional Compounding Centers of America
Who is PCCA – Professional Compounding Centers of America | Compounding Pharmacy Supplier.
Who regulates compounding pharmacies and how?
The practice of compounding is regulated by state boards of pharmacy. Community and hospital compounding pharmacists are allowed exemptions to the Federal Food, Drug, and Cosmetic Act of 1938 if they comply with the regulations outlined in Section 503A.
Does the FDA regulate compounding pharmacies?
Compounded drugs are not FDA-approved. This means that FDA does not verify the safety or effectiveness of compounded drugs. Consumers and health professionals rely on the drug approval process for verification of safety, effectiveness, and quality.
Which are the two primary regulators in compounding?
There are two primary sources for professional standards of drug compounding: the United States Pharmacopeia (USP) and a system of voluntary accreditation.
What standards are in the USP NF that pertain to compounding?
USP provides three types of public quality standards for compounding:
- General Chapters.
- Compounded Preparation Monographs.
- Monographs for Bulk Drug Substances and Other Ingredients.
- USP Healthcare Quality & Safety Standards-Setting Process.
What is the difference between a compounding pharmacy and a regular pharmacy?
The only real difference is that compounding pharmacies combine the ingredients in-house to meet the individual patient’s needs. Patients require a prescription for all compounded medications, just as they do for retail pharmaceutical prescriptions.
How do compounding pharmacies make money?
Rather than paying for a finished product, pharmacies buy compounding ingredients directly. The compounded medication offers higher margins for pharmacies because it requires fewer expenses to provide the product.
What is FDA 503B?
Section 503B(d) defines an outsourcing facility, in part, as “a facility at one geographic location or address.” FDA interprets “facility,” as used in this section, to mean a business or other entity under one management, direct or indirect, engaged in the compounding of human drug products.