The Latini is a company specialized in providing services of Regulatory Field, with thousands of approved processes. Founded in 1996, the company counts on a specialized technical staff allowing time reduction on process formulation, with gains of efficiency, time, cost and personal designated for this job.
Working in association with our clients’ Regulatory Affairs field, we analyze customized solutions, monitor the scenario and manage the inherent regulatory risks of each company activity. We have already served companies from more than 25 countries; and we have obtained the approval of thousands of products. We rely on strategic partnerships in Brazil and abroad, promoting the access of our clients to these global markets.
In contemporary globalized world, it is important to count on a strong partner in Regulatory Field in order to overcome the non-tax barriers and, to achieve markets by the increasing of companies' businesses.
Count on a strong partner. Count on Latini Group, expert in Regulatory Affairs.
A NEW VALUE PROPOSITION
From 2017, the brands of the Latini group are going to be consolidated into a single, more dynamic and current brand: the Latini Group.
Always acting in accordance with the Regulatory in Business, the group's companies have been helping our customers to add value, generate business and reduce regulatory risk.
With a strong concept in integrated solutions, our companies are able to generate competitive advantage for your business, saving time and financial resources, as well optimizing human resources, which are indispensable in the current competitive scenario.
Our teams are composed of high-level consultants and technicians with great professional experience in regulatory, life sciences and technology areas.
We have strategic partners located in every continent, allowing us to develop and manage projects in various countries with great commercial potential for our customers, whether between foreign countries, from Brazil to other countries or vice versa.
- Securities management;
- Full document management;
- Consulting and regulatory advice;
- Regulatory audits;
- Development and implementation of quality systems (GMP);
- Regulatory training.