SERVICES
Whichever stage you’re at, Activ Pharmaceuticals can help
At Activ Pharmaceuticals, we provide a comprehensive range of services catering to your needs with 2 optionsComplete suite of services from start to finish
or
Flexibility to select specific services as per your requirements
Formulation Development
Activ Pharmaceuticals has a dedicated in-house research and development facility, employing experienced formulation chemists. This department works closely with you to ensure commercial success of your finished product.
We can tailor a formula specifically for you, or supply a formula from our large database of products. Alternatively, we can develop a formulation based on your specifications.
Packaging Development
Choice and design of packaging is a primary consideration for any product that is offered for sale at retail level.
We can assist withChoosing the appropriate packaging to contain the product and also protect it during handling.
Providing packaging that is functional, appealing, and user-friendly.
Design or select a market pack that is acceptable to the retailer.
Selecting materials with minimal environmental impact or legal constraints.
Sourcing a cost-effective pack.
Filling & Packing
Our staff are highly trained using dedicated, modern technology during the filling and packing process to ensure product quality and consistency is maintained throughout.
Offering a wide range of fill volumes, we also cater for a large variety of formulations (very thin products to viscous gel and cream products).
We can manufacture the product for you, or you can supply your own bulk product for us to fill.
Activ Pharmaceuticals provide high quality contract manufacturing and packaging services that ensure your product stands out on the shelves!
Bulk Product Manufacturing
Activ Pharmaceuticals prides itself on delivering quality products consistently and on time. Once raw materials are received, Activ Pharmaceuticals can have finished goods ready for shipment within 4-6 weeks.
All equipment is cleaned, sanitised and inspected prior to manufacture. Dispensed raw materials are processed in accordance with approved and validated manufacturing procedures under clean room conditions to produce the bulk product.
The bulk is subjected to Quality Control testing and, provided the batch meets specifications, is approved for filling.
Storage & Delivery
Raw materials, packaging components, and finished goods are stored in a controlled and secure warehouse accessible only by authorised staff.
Activ Pharmaceuticals has an excellent record of consistently delivering products on time. We understand a customer's need to have products available for sale at all times and keep inventory at acceptable levels.
Records of all incoming and outgoing products are available for audit and review by the customer and/or the authorities. These records provide full product traceability and can be produced on demand.
The transport companies we choose to partner with are reputable reliable carriers for the safe delivery of finished goods.
Release for Supply
Activ Pharmaceuticals are licensed by the TGA to release therapeutic products for supply/sale. The Quality Assurance Manager or delegate, are the only persons authorised to conduct this function and will only do so when they have satisfied themselves that the product is 'Fit for Purpose'.
This service is offered to all our clients under the GMP Agreement between us.
Stability Testing
Activ Pharmaceuticals has the expertise and the necessary facilities to undertake accelerated and full-time stability studies. All new products are subjected to preliminary, accelerated stability testing, as well as preservative efficacy where appropriate. Full-time stability testing is conducted by individual arrangement.
Under current GMP guidelines, therapeutic products must be placed on a program of ongoing, stability studies. Activ Pharmaceuticals can assist with regulatory guidance.
Activ Pharmaceuticals may also conduct a stability program for the purpose of Listing or Registering a new therapeutic product. For these cases, we will generate the data and compile the finished report to the nominated regulatory affairs body for submission.
