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Overview and Purpose:
Teoxane Laboratories is an international pharmaceutical and medical aesthetics company specialising in the development of hyaluronic acid–based injectable products and professional skin solutions. Its portfolio includes prescription and professional-use products designed to support aesthetic and dermatological practice.
Engagement with Teoxane reflects a commitment to evidence informed product selection, structured clinical education, and adherence to manufacturer guidance within aesthetic practice.
Commencement:
Expires:

Regulatory or accrediting body:
Teoxane is a manufacturer and supplier of medical devices and aesthetic products. It is not a statutory regulator and does not confer professional licensure or authority to practise.
Its role is to support healthcare professionals through:
Research and development of hyaluronic acid technologies
Manufacture of CE or UKCA marked medical devices
Provision of professional training and clinical guidance
Product safety monitoring and technical support
Development of treatment protocols
This role complements, but does not replace, statutory regulation or professional registration.
Scope of recognition:
Association with Teoxane relates specifically to the use of its products and participation in its professional education pathways. This may include:
Access to professional-only injectable and skincare products
Training in product handling and clinical application
Protocol guidance and treatment frameworks
Ongoing professional education and updates
Technical and safety support
Such engagement does not constitute regulatory approval or professional accreditation.
Standards and core requirements:
Use of Teoxane products requires adherence to defined professional and safety standards, including:
Appropriate professional background and scope of practice
Completion of relevant product or protocol training
Compliance with medicines and medical device legislation
Adherence to manufacturer instructions and contraindications
Safe storage, handling, and traceability
Ethical representation of treatments
These standards are designed to promote consistency, safety, and responsible use.
Relevance to patient safety and public assurance:
Use of Teoxane products requires adherence to defined professional and safety standards, including:
Appropriate professional background and scope of practice
Completion of relevant product or protocol training
Compliance with medicines and medical device legislation
Adherence to manufacturer instructions and contraindications
Safe storage, handling, and traceability
Ethical representation of treatments
These standards are designed to promote consistency, safety, and responsible use.
How the clinic meets these requirements
The clinic integrates Teoxane products within its governance framework by:
Using authorised supply chains for product procurement
Ensuring practitioners complete relevant product training
Following manufacturer guidance and clinical protocols
Maintaining documentation of training and competence
Incorporating products into consent and treatment pathways
Reviewing outcomes and safety data
This ensures product use remains appropriate, traceable, and governed.
Monitoring, review and ongoing compliance:
Use of Teoxane products is reviewed as part of routine governance activity, including:
Monitoring updates to product guidance or safety notices
Reviewing training and competency records
Auditing storage, traceability, and documentation
Reviewing incident reports and learning outcomes
Updating internal protocols where required
This supports continuous improvement and patient safety.
Transparency and verifications:
Use of Teoxane products and professional engagement may be verified through supplier documentation, training certificates, and purchasing records.
Additional information can be provided via the clinic’s governance contact routes where appropriate.
Transparency and verifications url:



