New product development (NPD) for supplements and listed medicines

New product development (NPD) and existing product development (EPD) for supplements and listed medicines: formula manufacturability, dosage form, pack format, trial batches and scale-up in Sydney.

Our product development team helps turn a concept or an existing formula into a product that runs reliably in production and looks right in its pack. We work on capsules, tablets, powders, liquids and creams at our TGA GMP licensed facility in Kings Park, Sydney.

New product development (NPD)

  • Turning your concept into a workable formula and dosage form

  • Choosing excipients, fill weights and capsule or tablet sizes

  • Pack format and presentation

  • Trial or pilot batches before commercial runs

Existing product development (EPD)

  • Moving an existing product to us from another manufacturer

  • Reformulating for better flow, fill or tablet quality

  • New pack formats or sizes for an existing product

  • Scaling a small-run product to larger volumes

How development runs

  1. Brief and NDA

  2. Manufacturability review and quote

  3. Trial batch and your approval

  4. Specification sign-off

  5. Commercial manufacture and packing

Related

Launch a supplement brand · Small batch manufacturing · Guide: capsules, tablets or powders

Regulatory responsibility: the brand owner (sponsor) is responsible for the product’s regulatory status, ingredients, claims and labels. We manufacture to the specification you approve and do not provide regulatory, claims or labelling advice.

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The information on this website is general in nature. It is not regulatory, legal or medical advice. DB Pharmaceuticals manufactures products to the specifications approved by each brand owner, who is responsible for their product's regulatory status, claims and labelling.