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
- Veterinary Drugs
In addition to automated production lines, the following fully developed departments are in operation:
Quality Assurance and Quality Control Departmentsfeaturing completely equipped Microbiology and Chemistry laboratories.
Storage areaswarehouses with specially designated areas for the proper storage of raw materials, excipients, packaging materials and finished products.
Auxiliary areassupporting 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.