We make it simple
The import, export, or sale of food and drugs involves a complex process of analysis that determines the actual value of a product in this very legally-diverse market.
If you work in this area, you should know that Inventa works with experts who contact local agencies, public health authorities, and distribution associations. This allows your products to enter the market, complying fully with legislations concerning the testing of food and drugs.
How can we help
Inventa guarantees you a comprehensive consulting service throughout the food and drugs approval process. This service involves a careful analysis of your product, frequent state-of-play updates after consultations with public authorities, and reports indicating any adjustments needed to ensure your business is perfectly in line with the legal framework.
The service will help prevent and reduce the risk of problems that may affect the validity of your products on the market and in various other areas.
In addition to all of this, we also ensure the greatest possible monitoring of any legal and legislative changes that may affect your products and business. We also provide the necessary advice to proceed in accordance with local jurisdiction.
Our experts are highly experienced and skilled in the industry and guarantee you a personalized and focused support service. This service has four stages (which may vary according to each country's legislation):
Additionally, this service should be complemented with a trademark application (link to service page) as, in certain jurisdictions, this is a requirement for granting food or drugs approval.
This process, dedicated to the approval of food and drugs, is always supported by the guarantee of complete confidentiality and transparency every step of the way.
What is food and drugs approval and how does it work?
Food and drugs approval is a process by which government institutions assess, test, and approve a range or line of food or drugs, including medical devices. This process involves calculating the relationship between the benefits of the approved products and the potential risks of their use or consumption.
Why is food and drugs approval necessary?
Food approval is a public health matter, which means it requires a quality, safety, and efficacy assurance check on products of human or veterinary use - the same goes for drugs approval – thus helping protect those who purchase your products. Furthermore, the food approval system helps to advance public health as it accelerates the development of innovations responsible for making food and drugs safer and more accessible.
Additionally, in certain jurisdictions a trademark application is necessary before the food and drugs are approved for marketing.
How can Inventa help me with this?
Here at Inventa, we are perfectly qualified to offer you the maximum help when contacting regulatory agencies, public health authorities, and professional associations in the industry. We support you throughout the process of introducing your products onto the market by monitoring the current regulations and local standards on making, labeling, and marketing your goods and products in these sectors.
In brief, we can assure you consulting services on the approval and the development of your products, as well as the limitations to your marketing strategy for new or generic drugs, medical devices, and tobacco products. Our team is perfectly qualified to represent our clients in front of the regulatory organizations in this sector, as we combine the acquired knowledge about this complex market with a high capacity for reaction to adversity throughout the process.
For this reason, Inventa provides a fully-dedicated and qualified team to ensure our customers the most efficient, competitive, and profitable support in the regulating and leveraging of their products. Contact us to learn more about how we can ensure maximum defense and protection for your business.
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