Manufacturing Operations

We are authorized to manufacture non-sterile medicines, food supplements, medical devices, cosmetics and body care products.

We are authorized by Infarmed to produce non-sterile medicines in the following dosage forms:


  • Tablets;
  • Hard capsules;
  • Dragees;
  • Powders;
  • Granules;


  • Lotions;
  • Ointments;
  • Gels;
  • Pastes;


  • Solutions;
  • Syrup;
  • Drops;
  • Suspensions;
  • Elixirs;

In addition to medicines, Lecifarma has skills and equipment to produce a wide range of products, of which we highlight food supplements, cosmetics and body care products.

In this way, there are several manufacturing operations performed at Lecifarma, such as:

We have suitable means and equipment to guarantee the packaging of the products in accordance with Good Manufacturing Practices and ensure their quality in all stages of manufacture.


  • Industrial Exploration License
  • Manufacturing Authorization
  • GMP Certification (Good Manufacturing Practices)

Quality Control

At Lecifarma we have as priority the quality, safety, efficacy and credibility of our products. In this context, the Quality Control Department encompasses microbiological and physicochemical analysis of raw materials, bulk, intermediate product, packaging materials and finish product. This Department plays a key role in assuring our customers as well as the final consumer the highest quality standards through compliance with Good Manufacturing Practices (GMPs). Accurate specific analysis, carried out by highly qualified technicians, allow us to achieve the quality and safety required in this branch of activity..