Practitioners who document supplement recommendations as part of patient care often ask how to properly note this in patient charts — particularly for products recommended through a dispensary model like SHS rather than prescribed medications. Here’s a practical framework.
Why Documentation Matters
Supplement recommendations, while not prescriptions, are still part of your clinical decision-making and patient care plan. Documenting them serves several purposes: continuity of care if the patient sees another provider, a record for your own reference on what’s been tried and when, and — for practitioners in states or practice types where it applies — supporting documentation for the clinical reasoning behind a recommendation.
What to Include in a Chart Note
- Product name and specific formulation — e.g., “Scientific Health Solutions Melatonin 60mg” rather than just “melatonin,” since specificity matters if the patient needs to reorder or if outcomes are being tracked
- Date of recommendation
- Brief clinical rationale — why this recommendation, in the context of the visit
- Any relevant lot number or COA reference — if you’re tracking quality documentation, noting which batch was recommended provides a traceable record
- Follow-up plan — when you’ll reassess
Using Your Practitioner Code as a Reference Point
Since patients order directly using your unique SHS practitioner code, your account provides a record of what’s been ordered under your recommendation — a useful cross-reference against your own chart notes if you need to verify what a patient actually purchased versus what was initially recommended.
COA Documentation for Your Records
If you maintain detailed supplement documentation, you can request a Certificate of Analysis for the specific lot number a patient received and keep it on file alongside your chart note. This provides a complete record: recommendation, rationale, specific product and lot, and quality documentation for that lot — useful for practitioners who want a thorough paper trail for the supplements they recommend.
This is general practice guidance, not legal or compliance advice specific to your state or practice type — consult your practice’s compliance resources for documentation requirements specific to your situation.
Register as a Practitioner | Related: Supplement Quality Documentation: COAs, Lot Numbers & Batch Testing