ProRx Pharma Achieves DEA Registration for Controlled Substances

ProRx Pharma Achieves DEA Registration for Controlled Substances

Certification Expands Capabilities, Strengthens Compliance, and Supports Provider Partnerships

ProRx Pharma, a notable player in the health and wellness outsourcing sector, has received a DEA Controlled Substances Registration Certificate. This important achievement allows the company to manage and distribute specific controlled substances, broadening the scope of compliant, high-quality medication it can provide to healthcare providers.

According to Kurt Lunkwitz, the chief operating officer at ProRx, "Earning our DEA Controlled Substances Registration Certificate is a pivotal moment for ProRx. It not only enables us to expand into compounding and distributing Schedule III substances like testosterone, but also demonstrates our commitment to regulatory excellence. This certification strengthens our ability to serve providers with trusted therapies, expand partnerships, and support long-term business growth." This commitment emphasizes ProRx's strategic focus on delivering effective healthcare solutions.

A Schedule III substance, according to the Controlled Substances Act (CSA), is noted for having a moderate potential for physical or high psychological dependence. However, it is recognized for its medical uses in the United States and has a lower abuse potential compared to Schedule I and II substances.

The DEA Controlled Substances Registration Certificate, which is issued by the U.S. Drug Enforcement Administration, is crucial in regulating and overseeing the manufacturing, distribution, or dispensing of controlled substances. This certificate signifies that ProRx has successfully complied with extensive federal security, recordkeeping, and accountability requirements. Achieving this status allows ProRx to confidently support healthcare providers with essential medications that require DEA oversight.

In addition to securing the DEA Controlled Substances Registration, ProRx also maintains consistent compliance with other important regulatory frameworks, including:

Additional Regulatory Compliances

• FDA 503B Outsourcing Facility Registration
• State Board of Pharmacy Licensure
• cGMP Compliance

About ProRx
ProRx is an FDA-registered, cGMP 503B outsourcing facility dedicated to providing safe, compliant, and high-quality compounded sterile and nonsterile preparations to physician practices, medical clinics, and med spas across the country. With a strong focus on preventative health, regulatory excellence, reliability, and customer service, ProRx establishes partnerships with healthcare providers to ensure access to necessary therapies for patients. ProRx is committed to fostering a supportive environment for healthcare excellence.

Frequently Asked Questions

What is the significance of the DEA Controlled Substances Registration Certificate?

This certificate allows ProRx Pharma to handle and distribute controlled substances in compliance with federal regulations, enhancing their service offerings.

What types of substances can ProRx distribute with this certification?

ProRx can compound and distribute Schedule III substances, which may include medications like testosterone.

How does ProRx ensure compliance with regulations?

ProRx adheres to strict regulatory standards, holding certifications such as FDA 503B Outsourcing Facility Registration and cGMP Compliance.

Why is the registration critical for healthcare providers?

The DEA registration allows healthcare providers to access a wider range of compliant and high-quality medications, ultimately improving patient care.

What is the primary focus of ProRx in terms of healthcare delivery?

ProRx prioritizes preventative health and reliable customer service, ensuring providers have access to necessary therapies for their patients.

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