Cosmepeutics International Pty Ltd understands the need for complete confidentiality especially when handling formulations, clinical evidence and manufacturing details, on your behalf.
We have a standard confidentiality contract that requires the signatures of both parties. This is designed to protect you, our client, so you can be sure the only information shared with others outside the business is the information you want shared.
We specialise in the development of a complete range of dosage forms including:
As you can understand, a successful outcome of unique product development depends on complete information provided in the Development & Design Brief.
If you are requesting unique product development or a new product form, we need to know if you, the client, have specific requirements including a detailed ingredient and packaging requirements. This is to include all the things that you would like in your product. You will be asked if you, the client, are supplying any of the specific raw materials or if we are sourcing these for you. Please keep in mind we may need to purchase the minimum amount from the alternative company and you may be billed for this, even if the total amount of the special order is not used.
If you only have a very basic idea, we can help you along. Our team of specialist chemists and marketers can create a special product just for you.
Many products undergo updates during their product life cycle. These changes may be to reduce manufacturing costs or change a product’s image or functionality. By revamping older products, these changes will help preserve market share and extend the life cycle of many products.
We can work with you in this regard to maximize your investment.
We recommend that any new formulation development include a preservative efficacy test to ensure long term safety and stability. This is arranged through well-known, reputable experts in this field.
Through our associates we can offer a suite of dermatological tests such as Clinical Trials on all actives;
Our consulting regulatory expertise can assist with product registration including TGA and APVMA in Australia and overseas authorities including European Reach, US FDA and many Asian countries.
A quote, based on the particular requirements, can be provided.
A lecture program for staff or customer education can be created specifically for your purpose and delivered at your premises or at a venue of your choice.
These are conducted on laboratory batches to determine if they are stable enough for cosmetic applications or if they are to be submitted for Long Term Stability Trials.
Note; Cosmetic and Cosmeceutical products may not require development and validation of analytical methods, behnce these fees may not apply. Stability trials in these cases are based on physical testing only.
Also, standard sunscreen formulations based on known sunscreen actives, may also have the development and validation of analytical methods wavered.
Stability testing according to TGA, ICH or other appropriate Guidelines, can be arranged, at 5oC, 25oC, 30oC (including 30oC / 75% RH and 30oC / 65% RH) and 40oC; for 6 months to 5 years, depending on regulatory requirements.
Supply and execution of method transfer protocols. Expert regulatory documentation created for regulatory submissions worldwide.
If full scale stability testing (including development and validation of analytical methods) is required a quote from an accredited laboratory can be obtained and provided to you. This will be without additional charges from us.
We will let you know all details in advance and charges will be discussed at that point in time.
Disclaimer; If no stability testing has been carried out on the product, Cosmepeutics International Pty Ltd will take no responsibility for the integrity of the product. This includes physical testing, chemical testing (where required) and a Preservative Efficacy Test as a minimum.
Often small scale manufacturing is required for cosmetic products for test markets or niche products. Batches from our formulation range or yours in quantities of up to 150Kg, in bottles, jars or tubes, can be manufactured.
Once a prototype formulation has been agreed to, our laboratories can prepare sufficient product to enable samples for stability studies, clinical trials or small scale marketing evaluation, as required.
Our formulation team require between 14 – 28 days to review and price products with standard raw materials.
Should specialized raw materials be required this may be longer depending on sourcing of these components. Please also note that the more products in the range, the longer this can take.
We aim to give you the best service possible and will work closely with you to ascertain you needs are being met. To do this we have minimum quantity requirements on our manufacturing facilities – these are generally 5- 20Kgs (filling would suit production batch sizes). Please note however costs are dependant largely on batch size with smaller quantities being more expensive per unit produced.
Quotes on production of larger quantities can be provided (if required) from reputable contract manufacturers. We will endeavor to match your requirements with the most appropriate contractor.
