$ 1 ,706.00 Original price was: $ 1 ,706.00.$ 697.00Current price is: $ 697.00.
Structured documentation for clinics offering IV vitamin therapy and infusion services. Nine templates covering patient information, consent, intake screening, treatment records, emergency protocols, scope of practice, compounding policy, aftercare, and TGA compliance.
• IV therapy patient information sheet and informed consent
• Health screening and intake form specific to infusion therapy
• Treatment record template for ongoing patient documentation
• Emergency protocol for adverse infusion reactions
• IV compounding and preparation policy
• TGA compliance checklist and mobile IV service terms
IV infusion clinics, vitamin therapy providers, wellness clinics offering drip therapy, and mobile IV service operators setting up compliant clinical workflows.
Use when launching an IV infusion service, adding mobile IV to your offerings, training new infusion staff, or preparing for a TGA compliance review of your infusion operations.
Point-in-time document bundle at date of purchase. Customise each template for your jurisdiction, services, and clinical context before use. Not legal advice. Membership tier includes ongoing updates as regulations change.
A professional handout that explains IV vitamin therapy to patients before their first appointment. Sets realistic expectations about what the evidence says and what the experience involves.
A professional handout that explains IV vitamin therapy to patients before their first appointment. Sets realistic expectations about what the evidence says and what the experience involves.
IV clinics, mobile IV providers, and integrative medicine practices.
Send before the first IV appointment. Manages expectations and reduces clinical risk by surfacing contraindications early.
Point-in-time document at date of purchase. Customise for your jurisdiction, services, and clinical context before use. Not legal advice. Membership tier includes ongoing updates as regulations change.
Consent designed specifically for IV infusion. Covers the risks of intravenous administration that a general consent form does not address, and makes clear that results are not guaranteed.
Consent designed specifically for IV infusion. Covers the risks of intravenous administration that a general consent form does not address, and makes clear that results are not guaranteed.
All IV therapy providers including in-clinic and mobile services.
Required at every IV session. Re-sign when changing formulation or adding new ingredients to the patient's regime.
Point-in-time document at date of purchase. Customise for your jurisdiction, services, and clinical context before use. Not legal advice. Membership tier includes ongoing updates as regulations change.
Screen patients before their infusion, not after a complication. This form identifies contraindications, allergies, and medical conditions that should trigger a pause or a referral.
Screen patients before their infusion, not after a complication. This form identifies contraindications, allergies, and medical conditions that should trigger a pause or a referral.
IV clinics and mobile IV providers conducting new patient screening.
Use at every new IV patient consultation. Refresh every 12 months and any time the patient's medical status changes.
Point-in-time document at date of purchase. Customise for your jurisdiction, services, and clinical context before use. Not legal advice. Membership tier includes ongoing updates as regulations change.
<p>A clinical record for each infusion session. Captures batch numbers, infusion rate, vital signs, and observations so every treatment is documented to the standard a regulator would expect.</p>
A clinical record for each infusion session. Captures batch numbers, infusion rate, vital signs, and observations so every treatment is documented to the standard a regulator would expect.
RNs and other clinical staff administering IV therapy.
Use at every IV session. Forms part of the legal medical record and is the first document reviewed in any complaint.
Point-in-time document at date of purchase. Customise for your jurisdiction, services, and clinical context before use. Not legal advice. Membership tier includes ongoing updates as regulations change.
<p>When a patient reacts during an infusion, your team needs a protocol on the wall, not a policy in a drawer. Step-by-step responses for anaphylaxis, extravasation, and vasovagal episodes.</p>
When a patient reacts during an infusion, your team needs a protocol on the wall, not a policy in a drawer. Step-by-step responses for anaphylaxis, extravasation, and vasovagal episodes.
All IV clinics and mobile IV providers.
Train every IV nurse at induction and confirm competency every 12 months. Use as the immediate bedside reference.
Point-in-time document at date of purchase. Customise for your jurisdiction, services, and clinical context before use. Not legal advice. Membership tier includes ongoing updates as regulations change.
<p>Who in your IV clinic can cannulate, administer, and supervise? This policy draws clear lines based on qualifications and training so everyone knows their role and their limits.</p>
Who in your IV clinic can cannulate, administer, and supervise? This policy draws clear lines based on qualifications and training so everyone knows their role and their limits.
IV clinics with mixed RN, EN, and medical practitioner workforces.
Use to define who can do what. Critical for nurse-led IV models with medical oversight.
Point-in-time document at date of purchase. Customise for your jurisdiction, services, and clinical context before use. Not legal advice. Membership tier includes ongoing updates as regulations change.
<p>If your clinic prepares its own IV infusion solutions, you need documented procedures covering sterile technique, ingredient verification, and TGA manufacturing requirements. This policy covers it all.</p>
If your clinic prepares its own IV infusion solutions, you need documented procedures covering sterile technique, ingredient verification, and TGA manufacturing requirements. This policy covers it all.
IV clinics compounding their own infusions and clinics receiving compounded products from external pharmacies.
Use to align with the TGA’s position on cosmetic compounding. Particularly relevant given recent regulator focus.
Point-in-time document at date of purchase. Customise for your jurisdiction, services, and clinical context before use. Not legal advice. Membership tier includes ongoing updates as regulations change.
<p>Taking IV therapy to patients’ homes or offices? These terms cover the unique risks and responsibilities of off-site service delivery, from venue suitability to emergency response.</p>
Taking IV therapy to patients’ homes or offices? These terms cover the unique risks and responsibilities of off-site service delivery, from venue suitability to emergency response.
Mobile IV operators delivering services in homes, hotels, events, and corporate settings.
Use as the standard terms for mobile IV bookings. Reduces venue-related risk and disputes.
Point-in-time document at date of purchase. Customise for your jurisdiction, services, and clinical context before use. Not legal advice. Membership tier includes ongoing updates as regulations change.
<p>A take-home sheet patients actually read. Covers what is normal after an infusion, what is not, and when to call your clinic or head to the ED.</p>
A take-home sheet patients actually read. Covers what is normal after an infusion, what is not, and when to call your clinic or head to the ED.
IV clinics issuing post-treatment guidance to patients.
Issue at the end of every IV session, in print and digital format.
Point-in-time document at date of purchase. Customise for your jurisdiction, services, and clinical context before use. Not legal advice. Membership tier includes ongoing updates as regulations change.
<p>A self-audit checklist for your IV clinic’s TGA obligations. Covers ARTG listings, advertising compliance, supply chain documentation, and the labelling requirements that catch operators off guard.</p>
A self-audit checklist for your IV clinic’s TGA obligations. Covers ARTG listings, advertising compliance, supply chain documentation, and the labelling requirements that catch operators off guard.
IV clinic owners, clinical leads, and compliance contacts conducting an annual TGA review.
Use as a self-audit before any TGA inspection or as a quarterly governance tool.
Point-in-time document at date of purchase. Customise for your jurisdiction, services, and clinical context before use. Not legal advice. Membership tier includes ongoing updates as regulations change.
Compliance and governance support grounded in the realities of Australian cosmetic practice.

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