Through Drug Qualification studies, we have been able to broaden the specification of impurities in pharmaceutical products and thereby help our business partners to establish an accurate risk analysis based on toxicological data, helping them to avoid reformulation.
Learn about the advantages of our service
Helps avoid rephrasing | Through the qualification of impurities, it is possible to know whether or not there is a risk that they are harmful and, above all, at what concentration, so that products can have broader specifications based on reliable information. |
Saves time | The average turnaround time is 30 to 45 days. According to data obtained in conjunction with our business partners, we know that a reformulation requires 8 to 24 months. |
Lower cost | According to studies carried out in conjunction with our clients, it is known that a reformulation has a cost of between 2 and 5 million pesos, the qualification service is only a fraction of these costs. |
Almost immediate information with international validity | The most important advantage is that our customers can make decisions based on toxicological data, so they can continue with the registration of their products. Because qualification studies are carried out in compliance with international standards, the results obtained are valid in different regions of the world. |