Complementary Medicines Group (CMG) is a multi award winning, Therapeutic Goods Administration (TGA) registered Australian contract manufacturer in the complementary medicine and food industries.
Through a collaborative, gated development process, we place our customers at the centre of every key decision, delivering market ready products built on science, innovation and quality.
CMG has simplified the complex path from initial product concept to finished, market ready goods through the CMG Chevron – a structured framework that guides customers through DESIGN, DEFINE, and DELIVER.
By combining deep technical expertise with clear decision points and customer approvals at every stage, we reduce risk, improve transparency, and ensure products are delivered in an efficient, timely manner, built on science, innovation, and quality.
During the DESIGN stage, CMG works closely with customers to transform their product concept into a viable, physical solution.
We develop TGA compliant product formulations and flavour samples for customer review and approval, ensuring the concept is technically sound and commercially feasible.
To support confident decision making at this early stage, CMG also provides clear guidance on product costs, minimum order quantities, and indicative delivery timeframes.
Progression beyond DESIGN occurs only after customer approval and receipt of a purchase order, ensuring transparency and controlled commitment.
In the DEFINE stage, CMG collaborates with customers to complete the detailed due diligence required to convert the approved concept into a regulatory ready, saleable product.
Our regulatory expertise is applied throughout this phase with customer input and approvals sought as we progress through bulk material selection, evidence packages, Australian Register of Therapeutic Goods (ARTG) listing (where applicable), product stability program, packaging design, and labelling.
To minimise delays to market, CMG procures raw materials, packaging components and labels as soon as customer approvals are received.
In the DELIVER stage, CMG manufactures market ready products within a robust quality and compliance framework at our state of the art, TGA registered facility in Sydney’s Northern Beaches.
Operating in accordance with Good Manufacturing Practices (GMP), independent testing and stringent quality assurance checks are applied throughout manufacturing and packing, ensuring every finished product meets the highest quality standards.
CMG has expertise in manufacturing, product development, regulatory and stability services, and labelling and packaging.
Manufacturing across multiple dosage forms:
End-to-end product development services:
Regulatory and Stability services:
• Compliance with permitted ingredients and regulations
• Evidence Tables and Evidence Packages
• Australian Register of Therapeutic Goods (ARTG) listing submissions
• Stability testing
Labelling and Packaging:
Our Experience and Industry Leadership:
For more information on new product development or for manufacturing your products, contact us at info@cmgrouponline.com.au