FDA regulations

COMPOUNDING SIG: To 503B or Not to 503B: That is the Question?

2026-10-07T16:23:22-05:00September 15th, 2026|Categories: 503B, Business, Compliance, compounding, Compounding SIG, FDA, Outsourcing Facility, Pharmacy Law, Pharmacy Practice, Regulatory Issues|Tags: , , , , , , , , , , , , , , , , , , , , , , |

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Should your pharmacy consider 503B outsourcing? What are the opportunities, costs, and regulatory considerations?

Join us for a discussion of the 503B outsourcing facility model and how it differs from traditional pharmacy compounding. We’ll explore the current 503B market, capital and operational requirements, regulatory differences, and important considerations for pharmacies evaluating whether 503B may be right for their business.

The discussion will also include a separate look at controlled substances and the additional regulatory requirements and considerations that apply.

Whether you are considering entering the 503B space, partnering with a 503B facility, or simply want to better understand the differences, this SIG will provide valuable insight to help you make informed decisions.

Join us for this informative and timely discussion on one of the important questions facing compounding pharmacies today.

Erik Tosh, RPh, FACA, brings more than 40 years of pharmacy experience and nearly five decades of experience in healthcare, with a career spanning hospital pharmacy, independent community pharmacy, pharmaceutical compounding, and industry leadership. His extensive compounding experience includes serving as Director of Operations for a large sterile compounding facility that later became registered as a 503B outsourcing facility. In that role, he oversaw operations that included production, regulatory and compliance activities, purchasing, shipping, and the preparation of high-risk compounded medications for hospitals across the United States.

Tosh later served as Vice President of Compounding Support Services at Letco Medical, where he led compounding support initiatives, developed continuing education programs, provided technical training, and worked closely with professional pharmacy organizations. He retired in 2021.

In addition to his industry experience, Tosh has served as adjunct faculty at Western University College of Pharmacy and has presented ACPE-accredited education on pharmaceutical compounding. He is a past President and Chairman of the International Academy of Compounding Pharmacists and has contributed to professional publications including Remington: The Science and Practice of Pharmacy and the International Journal of Pharmaceutical Compounding.

Considering the move to 503B? Join us for a discussion of what it takes to start or transition to a 503B Outsourcing Facility. We’ll begin with an overview of the key considerations involved, then open the conversation for attendees to ask questions, share experiences, and exchange perspectives.

This meeting will not offer CE.

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GLP-1 & Peptide Compounding CE: Legal and Regulatory Insights for Pharmacy Professionals

2026-03-20T09:44:50-05:00February 24th, 2026|Categories: Continuing Education, Compliance, compounding, On-Demand Webinars, Pharmacy Law, Regulatory Issues, Telemedicine / Telepharmacy|Tags: , , , , , , , , , , , , , |

Missed the live webinar on March 18, 2026? It’s now available on-demand so you can access the full program whenever it fits your schedule.

Earn 1.0 hour (0.1 CEU) of continuing education credit with this on-demand webinar focused on the evolving legal and regulatory landscape surrounding compounded GLP-1s and peptides.

This program reviews key considerations for 503A pharmacies, 503B outsourcing facilities, and telehealth providers, including FDA and State Board of Pharmacy enforcement, private litigation trends, and the impact of the GLP-1 shortage ending.

Participants will gain a clearer understanding of current prescribing, compounding, and promotional practices, along with practical steps to reduce regulatory risk and maintain compliance in a rapidly changing environment.

 

Q: Who should attend this webinar?
Pharmacists and pharmacy technicians involved in compounding, compliance, or telehealth services, as well as healthcare professionals interested in GLP-1 and peptide therapies.

Q: Will I earn CE credit?
Yes. This activity provides ACPE-accredited continuing education for pharmacists and pharmacy technicians.

Stay informed on FDA enforcement, private litigation, and telehealth risks impacting compounded GLP-1s and peptides.

REGISTER HERE!

Note: It is not necessary to create a Lecture Panda account to register for this webinar.


The American College of Apothecaries (ACA) is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. ACA has accredited this knowledge-based program for 1 contact hour (0.1 CEU) of continuing education credit for pharmacists and pharmacy technicians.

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