COURSE FORMAT

Home Study (24 hours) that reviews fundamental concepts in non-sterile compounding. The program concludes with a learning assessment and associated feedback.

INSTRUCTIONAL DESIGN

The Home Study is a comprehensive knowledge-based program that introduces core concepts and a set of practice tools that guide the Pharmacist and Pharmacy Technician in their day-to-day practice. Each section of the program concludes with a learning assessment, which also provides feedback to the learner.

DESCRIPTION

Today, operating or working in a compounding facility in the role of pharmacist or technician is more sophisticated. To distinguish your practice and meet the demands of this growing market, the adoption of a best practices model to manage a compounding pharmacy is essential. The implementation of best practices implies being efficient and effective (i.e., doing the right thing right). The overarching topics addressed in this program can be categorized into three components; standards of practice, business development, and compounding processes.

Implementing Standards of Practice

One of the primary objectives of this activity is to highlight the necessity of operating within a regulated and well-documented framework that adheres to established standards of practice. To do so, participants will learn how to practically implement and apply standard operating procedures, competency trainings, and ongoing compliance assessments with the fundamental philosophy of continuous quality improvement.

Business Development and Growth

A well-developed business acumen is also essential in operating a successful compounding practice. This activity will provide participants with applicable marketing and business strategies to kick-start or enhance their compounding practice. 

Optimizing Compounding Processes

Compounding process development brings together everything from the physicochemical properties, uses, and applications of raw ingredients to finished compounded preparations. The fundamental first steps of every compounding process is knowing what ingredient to select;  how to interpret and implement information found in a monograph and certificate of analysis; pharmaceutical calculations, including potency adjustments, salt-base conversions, water-content adjustments, among more. From here, participants will review key preparatory techniques and the integration of technology when formulating different non-sterile dosage forms (e.g., oral liquids, capsules, topicals, molded dosage forms, etc.). Lastly, emphasis will be placed on verification procedures to ensure the quality, safety, and integrity of the compounded preparation.

With these three foundational components, this activity provides participants with the fundamental tools and knowledge needed to meet current compounding practice requirements. By taking this activity, the participant will realize the value, and gain the necessary knowledge and skills, to adopt and implement a best practices model for years to come.