USP 800

Sterile Compounding Certificate Program | June 18–20, 2026

2025-12-15T16:08:04-06:00December 15th, 2025|Categories: Certificate Program, Compliance, compounding, compounding training, Continuing Education, Documentation, Hazardous drug handling, Pharmaceutical Training, Pharmacist Training, Pharmacy Law, Pharmacy Technician, Quality Assurance, Regulatory Issues, Sterile Compounding, USP 797, USP 800|Tags: , , , , , , |

The Comprehensive Sterile Compounding Certificate Program is a live, in-depth training program designed for pharmacists and pharmacy technicians involved in sterile compounding. This certificate-based course provides a structured, practice-focused review of sterile compounding standards, regulatory requirements, documentation, training, and quality systems to support safe and compliant operations.

Participants will examine the legal and regulatory framework governing sterile compounding, including applicable FDA guidance and key USP standards such as USP <797> and USP <800>. Emphasis is placed on understanding how these requirements translate into daily practice and inspection readiness.

The program includes detailed instruction on documentation, quality assurance and quality control programs, policies and procedures (SOPs), and personnel training and competency requirements. Attendees will review expectations for facility design, environmental monitoring, equipment, and workflow as they relate to sterile compounding compliance.

A focused module on hazardous drug handling addresses facility requirements, engineering controls, PPE, personnel training, and assessment of risk, with alignment to current safety and regulatory expectations.

This certificate program combines didactic instruction and application-based learning, offering attendees the opportunity to strengthen their sterile compounding knowledge while reinforcing compliance, safety, and best practices.

Advance your sterile compounding knowledge and compliance skills with this comprehensive, certificate-based training program for pharmacists and pharmacy technicians. Registration is below.

What attendees said:

  • “This class was super helpful in increasing my knowledge and technique in the lab. I highly recommend it.”
  • “It’s a great class! Anyone want to get into sterile or the ones already doing it, should really consider taking this class.”
  • “With nearly 20 years of sterile compounding practice and exposure, this course reinforced my knowledge and skills in this area. I am more confident after this course.”
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Fundamental Compounding with Pharmacy Law | March 19–21, 2026

2025-12-15T15:58:45-06:00December 15th, 2025|Categories: Continuing Education, Compliance, compounding, compounding training, Hazardous drug handling, Pharmaceutical Training, Pharmacist Training, Pharmacy Law, Pharmacy Practice, Pharmacy Technician, Regulatory Issues, USP 795, USP 800|Tags: , , , , , , |

Fundamental Compounding with Pharmacy Law is a live, multi-day compounding course designed for pharmacists, pharmacy technicians, and pharmacy professionals seeking a strong foundation in both compounding practices and regulatory compliance. This course integrates compounding principles with pharmacy law to support safe, compliant, and high-quality compounding operations.

Participants will review the regulatory framework governing pharmacy compounding, including applicable federal and state considerations and key United States Pharmacopeia (USP) standards. Emphasis is placed on documentation, quality assurance, policies and procedures, and compliance requirements essential to day-to-day compounding practice.

The course includes instruction and hands-on training in common nonsterile dosage forms, such as capsules, molded dosage forms, and topical preparations. Participants will learn proper techniques, equipment use, quality control measures, and best practices to support consistency and patient safety.

A dedicated session on hazardous drug handling addresses requirements for facilities, engineering controls, PPE, and personnel training, with alignment to applicable USP standards and safety expectations.

This program combines didactic instruction and application-based learning to reinforce compounding knowledge, regulatory awareness, and practical skills in a structured, in-person environment.

Build a strong foundation in compounding and pharmacy law with this comprehensive, live training designed for pharmacists, pharmacy technicians, and pharmacy professionals. Registration is below.

What attendees said:

  • “The ACA Fundamentals of Compounding Course was one of the best decisions I’ve made for my pharmacy. The small, hands-on setting, focus on USP 795/800, and opportunity to network with both new and experienced compounders made it invaluable. Highly recommend!”
  • “The instructor effectively highlighted important topics and used real-world examples to support learning. The small class size made it easy to ask questions and have open discussions.”
  • “The class was great. The networking with other pharmacists from different areas was great. I was immediately able to take the knowledge learned and apply it in my store.”
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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 application/certificate-based program for 21 contact hours (2.1 CEUs) of continuing education credit for pharmacists and pharmacy technicians.

2025 American College of Apothecaries Conference & Expo

2025-10-31T02:13:11-05:00April 28th, 2025|Categories: Continuing Education, ACA Fellows Benefit, Administration/Management, Community Pharmacy, Compliance, compounding, DEA, Ethics, FDA, Fellows and Members, Fellows Benefit, Member Benefits, networking, News Release, Pain Management, Patient Care, Patient Safety, Personal Development, Pharmacists, Pharmacy Law, Pharmacy Practice, Pharmacy Technicians, Preceptor/Mentor Training, Professional Development, Professional Growth, Public/Community Health, Regulatory Issues, Revenue, Risk Management, Sports Medicine, Telemedicine / Telepharmacy, USP 795, USP 797, USP 800, Veterinary Compounding, Webinar|Tags: , , , , , , |

It’s time to pack your bags and polish your business cards — the 2025 ACA Annual Conference & Expo is where independent pharmacy meets unforgettable opportunity!

📍 Memphis, TN | September 25–27, 2025

Join us at the legendary Peabody Hotel for the 2025 ACA Annual Conference & Expo — where independent pharmacy professionals come together to connect, learn, and grow.

Your registration includes:
• Continuing Education credit (except guest registration)
• Thursday Night Welcome Reception & Dinner
• All conference meals

• Full access to the exhibition hall

This is your chance to network with pharmacy leaders, discover the latest trends, and showcase your brand in a dynamic, in-person setting. With educational sessions, social events, and all meals included, this is more than a conference — it’s where pharmacy takes care of business!

Speakers Include:

Philip Cowley, PharmD
Kathy Campbell, PharmD
Jessica Beal, PharmD
Jennifer Adams, PharmD, EdD, FAPhA, FNAP
Sue Paul, RPh
L. Michelle Woosley, PharmD, MBA, CMAP

Reserve your spot today and be part of something meaningful!

2025 ACE Save The Date Rectangle
Reservations
The Peabody Memphis – The “South’s Grand Hotel”

The Peabody Memphis is legendary for its charm, elegance, gracious hospitality, and rich history. This Memphis icon, opened in 1869, is listed on the National Register of Historic Places and is world-famous for its five resident Mallard ducks, who march daily through the lobby at 11am and 5pm.

Nestled in the heart of downtown, this AAA Four-Diamond hotel offers a one-of-a-kind experience just blocks from Beale Street, the Memphis Rock ‘n Soul Museum, Fed-Ex Forum, Sun Studio, and the Orpheum Theatre.  The Peabody Memphis offers two Restaurants, two Bars, Spa, and a Deli with ice cream and desserts.

THE PEABODY MEMPHIS
149 Union Avenue, Memphis TN 38103

Group Rate: $249 plus taxes and fees
Room Block Deadline: Monday, August 25, 2025, at 5:00 pm CDT

To make your reservations, click the button below or contact Susan Decker, ACA Director of Conferences at 434-989-5938 or susan@acainfo.org.

Individuals will guarantee reservations with a credit card or deposit equal to the first night’s room and tax.

2025 Sponsors and Exhibitors

AirClean
Boiron
Gates
RX Insider
Topi CLICK
ZRT Lab

ACA HOME STUDY: Dermatological Compounding

2025-10-31T12:23:59-05:00April 16th, 2025|Categories: Continuing Education, compounding, Dermatology, Home Study, USP 800, Workplace Skills|Tags: , , , , , |

Our Dermatological Compounding Home Study is an accredited 5-hour knowledge-based program designed specifically for compounding pharmacists and pharmacy technicians. This self-paced learning program provides a thorough overview of the formulation and preparation of creams, emulsions, ointments, pastes, gels, PLOs, solutions, lotions, powders, and both semi-solid and commercially available bases.

Participants will also review important compendial standards, including microbial content, minimum fill, quality control, preparation and labeling, patient counseling, and guidelines for establishing and extending beyond-use dates.

Course Highlights Include:

Introduction to Compounding

  • History of pharmaceutical compounding
  • USP chapters and drug monographs
  • Best practices and evolving trends in the U.S.

Dermatological Disease States Covered:

  • Atopic Dermatitis (Eczema): Clinical features, treatment options, and custom formulations
  • Psoriasis & Cutaneous Infections: Includes dermatophytosis, candidiasis, and warts
  • Acne Vulgaris & Rosacea: Differentiation, treatment overviews, and compoundable therapies
Dermatological Compounding Home Study Logo

Whether you’re looking to strengthen your foundational knowledge or expand your skill set in dermatological compounding, this home study offers a well-rounded, practical approach. Enroll now and learn at your own pace! Registration is below.


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 5 contact hours (0.5 CEUs) of continuing education credit for pharmacists and pharmacy technicians.

Five Myths About USP

2025-11-02T21:37:40-06:00November 25th, 2019|Categories: USP 800|

By Ernest P. Gates. Jr., RPh, FASCP, FIACP, FACA
From THE VOICE OF INDEPENDENT PHARMACY, Fall 2019

For nearly 200 years, the United States Pharmacopeia – or USP – has been setting standards for pharmaceuticals and the practice of pharmacy. However, its latest chapter – like any new standard or regulation – is creating uncertainty among the pharmacy community. USP <800>, which governs pharmacy handling of hazardous medication, takes effect on December 1, and many states will require compliance as of that date.

There are many myths surrounding USP <800>. Below are five with which you should be familiar, to avoid falling into a trap of non-compliance with this important new chapter.

Myth: My pharmacy prepares hazardous drugs but I don’t need to make changes to my practice to comply.

Fact: USP <800> requires a lab with negative pressure ventilation, including a minimum of 12 air exchanges per hour. If you do not have a negative pressure lab to compound these drugs, and you are in a state that is enforcing USP <800>, or you ship to a state that is enforcing the chapter, you will need to cease operations until you have created such a facility. You should be aware that to create a negative pressure environment you will need to vent to the outside either through the roof or a side wall. This will require new ductwork or a relocation of your lab.

Myth: My state is not enforcing USP <800> so I am all set.

Fact: Even if your state is not implementing USP <800> as of December 1, you must be compliant to ship medication to any state that is enforcing it. If you are not compliant you must cease out-of-state shipping to these states until you bring your lab into compliance. Also, it is important to not rest on your laurels. Even states that do not plan to implement USP <800> by December will likely implement it eventually. Those pharmacies that first saw USP <800> approaching, or something like it, and built to that specification are in a much better place today. Even if it is not required now, you should plan as though it soon will be. Separate and apart from your board of pharmacy, the Occupational Safety and Health Administration (OSHA) has requirements for handling hazardous drugs that are in effect now.

Myth: USP <800> involves relatively quick fixes to my lab.

Fact: USP <800> compliance is anything but quick or easy. If you do not currently comply, you will need to install new equipment that must first be ordered and then professionally installed. Separate and apart from any equipment orders, you likely will need to make design and layout changes to your lab and pharmacy unless your facilities were built in anticipation of USP <800>. Design and layout changes can involve moving walls and replac-ing or installing new electrical and plumbing systems. If you have renovated any type of space before, including your kitchen or bathroom at home, you know how hard it is to get designs, bid out the work, hire a contractor and secure permits. You should not underestimate the time involved.

Myth: I am not concerned with USP <800> because I don’t compound.

Fact: All pharmacies – even retail only – must ensure compliance with USP <800>, in those states where it is being enforced. For instance, USP <800> has require-ments for handling finished dosage forms that are on the NIOSH Hazardous Drug List. A careful review of that list and USP <800> are necessary to ensure compliance. You can download USP <800> here.

Myth: If I am not compliant with USP <800> and I dispense hazardous drugs, my only concern is my state board of pharmacy.

Fact: Pharmacies that handle hazardous medications and do not comply are at risk of punitive action on multiple fronts. For example, an employee or former employee can allege harm to themselves or an unborn child and file a legal action. Also, OSHA always has the authority to issue stiff fines on the basis of an unsafe workplace.

Fortunately, you do not have to go it alone. There are consultants who can help navigate the thicket of regulatory and design issues to achieve compliance.USP <800> will create a safer workplace for you and your team. What we now know about hazardous drugs we didn’t necessarily know just a few years ago. Change is always hard, and sometimes costly, but it usually puts us in a better place when done.

Ernest P. Gates. Jr., RPh, FASCP, FIACP, FACA is President of Gates Healthcare Associates in Middleton, Mass. To learn more about Gates Healthcare Associates, or for help with USP <800> compliance, go to www.gatesconsult.com.

Ernie Gates

Ernest P. Gates. Jr., RPh, FASCP, FIACP, FACA

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