Setup Formulation Types?
Step-by-step instructions for configuring Formulation Types within SiCompounding.
Overview
Formulation Types define how compounded formulations are categorized, verified, controlled, and documented within SiCompounding. These settings control sterility requirements, verification steps, quality controls, and instruction templates used during compounding and release.
Formulation Types must be configured in Pharmacy Settings before compounding workflows can be used.
Accessing Formulation Types
Follow the steps below to navigate to the Formulation Types configuration screen.
Step-by-Step Navigation
- Click the FileMaker Pro icon to open FileMaker.
- When FileMaker opens, locate the large menu bar on the left side of the window.
- Click SiCompounding (near the top).
- In the next window, several icons appear across the middle of the screen.
- Select Pharmacy to open the Dashboard.
- From the blue sidebar menu, scroll to the bottom and click Settings.
- Under General Settings, select Formulation Types.
The Formulation Types window will appear.
Editing a Formulation Type
Each Formulation Type can be modified from the Actions menu.
Open the Edit Window
- In the Actions column, click the gear icon for the desired Formulation Type.
- A popup appears with two options.
- Select Edit to modify the selected Formulation Type.
- The Formula Type Information window opens.
Example: Inhalations Formulation Type
The example below shows the required data fields and configuration using Inhalations as a sample Formulation Type.
Basic Information
| Field | Value |
|---|---|
| Formula Type | Inhalations |
| Active? | Yes / No |
| Sterility | Sterile |
Additional Properties
| Property | Description |
|---|---|
| Time (Min) | Enter total time in minutes |
| Complexity | Color-coded scale from 1–5, with 5 being the most complex |
| Flavor Option? | Yes / No |
Default Verification List
The Default Verification List is used during Compounding Release.
- Click inside the field.
- Select one of the available verification processes.
- A sorted list of step-by-step verification requirements appears.
Example: Suspension Verification List
| # | Verification Step | Source Field |
|---|---|---|
| 1 | BUD (Correct and matching the printed labels) | BUD |
| 2 | pH | pH_Ending |
| 3 | Final Volume | BatchSizeProduced |
| 4 | Dose (Topic click, Pump) | UnitProducedQty |
| 5 | Labels (BUD, Lot Number, Ingredients, Product Name) | — |
| 6 | Controlled Substance Reconciliation (Signature) | — |
| 7 | Controlled Substance Reconciliation (Witness) | — |
| 8 | Physical Inspection (Color, Density, Clarity, etc.) | PhysicalDescription |
| 9 | Absence of Particles | QCElementPhyCharChecked_B |
| 10 | Closure Integrity | QCElementContainer_Checked |
| 11 | Storage Conditions | — |
Quality Controls
Each Formulation Type follows defined Quality Control requirements.
Example Quality Controls for Inhalations
- USP-71 – Method Suitability (Bioluminescence)
- USP-71 – Method Suitability (Compendial)
- USP-71 – Rapid Sterility
- USP-71 – Sterility (14 Days)
Formula Instruction Templates
Instruction templates define the step-by-step compounding process for the Formulation Type.
Example: Inhalation Template 1
| Step | Instruction | Requires ACK | Requires VER | Requires PHOTO |
|---|---|---|---|---|
| 1 | Weight out Ingredients | ✓ | ✓ | ✓ |
| 2 | Combine Drugs | ✓ | ✓ | |
| 3 | Fill Inhaler | ✓ | ✓ |
Saving the Formulation Type
Once all data has been entered:
- Click Save.
- You will return to the Formulation Types window.
Sorting and Viewing Changes
Sorting Records
- Click the Complexity column header to sort.
- Then click the Type column header for additional sorting.
Change Logs
- Select Change Logs to open the Record Modification Log.
- This window displays a history of changes made to Formulation Types.
- Click the X in the upper-right corner to close the window.
Pharmacy Settings Overview
The Pharmacy Settings section contains all templates and default configurations required for system operation and must be completed before using any other area of SiCompounding.
Configurable Areas Include
- Product settings
- Facility Areas
- Equipment
- Workflows
- Costs and Fees
- Lab Work
- COM Templates
- Notifications
- Integrations
- Access logs (via the Automations tab)
:::callout type="warning" It is critical to enter all available and required data for every section and subsection within Pharmacy Settings to ensure accuracy, compliance, and proper system behavior. :::
Summary
Proper setup of Formulation Types ensures:
- Accurate compounding workflows
- Consistent verification and quality control
- Reliable documentation and audit trails
Formulation Types should be reviewed and maintained regularly as pharmacy processes evolve.
Adding and Maintaining Equipment?
Step-by-step instructions for accessing, managing, and reporting equipment within SiCompounding.
Maintaining USP BUD Settings?
Step-by-step instructions for creating, editing, and maintaining USP Beyond-Use Date (BUD) settings for compounded sterile preparations in SiCompounding.