The following standard tests are available, including analytical reports, method statements and a 30 minute follow-up call to review results.
Subject experts in Regulations and Toxicology will produce a report with all of the relevant ingredient technical information listed in section 5 of the data dictionary (i.e. CAS numbers, REACH Registration etc.), and the toxicology related fields for each ingredient. You will be supplied with multiple pdf files containing ingredient data and toxicity files (CMR, CardioPulmonary, Addictive, Emissions and Other).
You will receive a checklist of all of the information required about the product. This is split into 2 parts: Part A (product information) and Part B (sales information). Our team will also answer any relevant questions.
We will audit your outer packaging, insert and primary packaging, and provide you with a report based on this review.
We will review your current product and create a simple description of the opening and refill mechanism. You will receive the completed description document ready for upload.
We will provide you with a checklist of all of the data required for your product notification. Then, when you provide us with the data, we will transfer it into the EU submission tool.
You will receive a checklist of all of the information required to enter your product design details. Our team will also answer any relevant questions.
We will provide a template for the design of the leaflet that must be provided with a product under TPD, and then perform a final review of your completed leaflet.
We will undertake full ISO 8317 child resistant testing on your container, and provide you with the Certificate upon successful completion of the testing.
Price breaks are available depending on the number of tests and services that you order.