GAP houses all its departments in its privately owned industrial park. GAP's plant operates in accordance with the latest international standards and builds upon state-of-the-art pharmaceutical know-how, technology and equipment, adhering to GMP and GLP requirements, therefore ensuring the qualitative superiority of its products.

GAP’s plant has five categories of production lines:

  • Soft capsules
  • Sustained release pellets
  • Tablets
  • Injectables
  • Veterinary Drugs

In addition to automated production lines, the following fully developed departments are in operation:

  • Quality Assurance and Quality Control Departments
    featuring completely equipped Microbiology and Chemistry laboratories.

  • Storage areas
    warehouses with specially designated areas for the proper storage of raw materials, excipients, packaging materials and finished products.

  • Auxiliary areas
    supporting the production processes and serving the staff.

To cap the entire production structure, GAP applies a Quality Certification procedure to all in-coming materials, to those being processed, produced and released from the production chain.

Controls include quality certification of all incoming materials, such as raw materials, excipients, packaging materials etc.

In-process controls are also carried out during the production process, to ensure the quality of the end product.

However, controls are not limited to the production processes; they extend to anything that could have a negative effect on product quality.

Therefore daily, constant controls extend to production equipment and monitoring of all areas and peripheral auxiliary systems related to ventilation, temperature, humidity, lighting etc.