A lot of our Customers order a document from our company confirming the quality of the products, specifically the "Act of Quality Control" or its equivalent (typically priced between 1000 and 1650 euros).
Our employees will evaluate the product's compliance with the necessary norms and standards of the country according to certain stages.
The product evaluation criteria can be selectively applied or modified based on our company's management decision. If you need more information or want to determine which criteria best suit your production before we start our partnership, please specify your preferences in our agreement that we provide via e-mail.
If no specific details are provided, we will proceed using the criteria we deem suitable for your product, chosen from the provided list based on our responsible team evaluation.
This list is indicative and varies depending on the product type, country, and needs, and it is carried out at the discretion of our firm. This type of analysis applies to all documents and contracts. The analysis is conducted in accordance with our firm's charter, management decisions, and the laws of the country where the firm is registered. Understanding and accepting this information is mandatory for cooperation with our firm.
List of process stages and steps of quality check:
A) Checking the product composition for exceeding the established norms of herbicides, etc.
B) Assessing the availability of similar products in the local market and their possibility of free circulation.
C) Conducting a comprehensive study of restrictions on product use in the market based on open source information, internet, etc.
D) Ensuring the absence of prohibited symbols and other restricted information on product labels.
E) Analyzing the composition of goods for exceeding the established norms of pesticides, identifying potential shortcomings, and suggesting methods for their elimination and prevention.
F) Checking for prohibited substances or narcotic components in the product composition.
G) Examining products for potentially hazardous or toxic organic compounds (if needed).
H) Ensuring the safety of equipment and its components (if samples are provided).
I) Analyzing public opinion on the internet regarding the demand for the checked products.
J) Identifying potential quality issues with the raw materials used to produce the products.
K) Verifying compliance of production equipment with technical and safety requirements for human life and health (only for equipment and medical devices).
L) Identifying potential issues among consumer groups of similar products in the target country.
M) Assessing the long-term use and operation of equipment and its analogues in local conditions and checking for contradictions with religious restrictions in the target country.
N) Analyzing compliance with storage conditions for food and other perishable goods in the target territory.
O) Verifying documentation for the presence of radioactive or other hazardous components.
P) Assessing the possibility of recycling failed equipment, including conditions and restrictions in the process in the target area.
A document issued by our responsible team - is based on the study of the above criteria does not require additional licenses and is provided in free form on the company's letterhead, featuring the coat of arms, flag, or attributes of the target country etc..
If Clients/Partners wish to clarify or order the full list of procedures, you must specify your requirements in written form in the signed contract with us (draft of contract and offer attached).