MADRID

MFG PLANT

Our Manufacturing Plants

The Farmalider Group has two manufacturing plants in Spain:

  • Farmalider MFG Plant Madrid
  • Farmalider MFG Plant Valencia

 

Both facilities are certified under GMP standards by the Spanish and International Health Authorities, have been audited by leading pharmaceutical companies, and employ highly qualified personnel.

As a trusted pharmaceutical CDMO, our manufacturing plants in Valencia and Madrid are established as ideal production partners for a wide range of pharmaceutical companies. Our comprehensive manufacturing processes and services respond to multiple industry needs.

Farmalider MFG Plant Madrid

Farmalider MFG Plant Madrid specializes in the manufacturing, handling, and packaging of pharmaceutical products in oral solid dosage forms, supplying over 50 international pharmaceutical companies.

Solid Dosage Forms:

Wet granulation products, Direct blends, Tablets, Film-coated tablets, Sugar-coated tablets, Hard gelatin capsules

Packaging formats:

Sobre

Sachets

blister_icon

Blisters

bote_icon

Bottles

Services

Manufacturing

  • Bulk and finished products
  • Pilot lots/variation lots

Packaging

  • Primary and secondary

Trials clinical trials

Analysis

  • Quality control and microbiology laboratories

Stability

  • Cameras for all climate zones

Development

  • Tailor-made products
  • Galenic formulations

Transfer

  • Technology
Farmalider

Facilities

  • Microbiology and physico-chemistry laboratory
  • Manufacturing plant with:
    1. Segregated wet and dry granulation areas
    2. Rooms designed for compression and coating of tablets 
    3. Encapsulation room for granulates and pellets 
    4. Six packaging lines for products in blister packs, sachets and bottles.
    5. Serialization lines
  • Climate-controlled warehouse

Certifications

Complies with the principles and guidelines of Good Manufacturing Practices (GMP).
The facilities are GMP-certified by the Spanish and International Health Authorities, undergo regular inspections, and have been audited by leading national and international pharmaceutical companies.

Production capacity

0

m2

0
tons/year
of wet granulation
Icono comprimido abierto
0
tons/year
of direct blends
0
million
tablets/year
0
million
capsules/year
Icono blister
0
blister packaging lines
with a total capacity of 80 million blisters/year

Key Pillars of Our Manufacturing Plants

Our facilities are designed to provide comprehensive, high value-added solutions throughout the entire product lifecycle — from development to final distribution. Each of our key pillars is focused on ensuring maximum quality, efficiency, and regulatory compliance, adapting to the specific needs of our clients and the most demanding international standards.

Regulatory Compliance and Guaranteed Quality

Our plants operate under the strict regulations of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP), in accordance with European legislation and WHO and ICH guidelines.
This ensures that all processes — from raw material reception to product release — meet the highest standards of quality and safety. We also implement a robust quality management system that includes process validation, change control, and periodic internal audits.

We apply lean principles to identify and eliminate waste within our production processes, improving efficiency and reducing costs.

Our advanced resource planning system enables efficient management of production, inventory, and distribution.
This allows us to align resources with actual market needs, avoiding both overproduction and shortages. We also maintain constant communication with our clients to anticipate and adapt to changes in demand.

Our plants operate under strict Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) regulations, in accordance with European legislation and WHO and ICH guidelines. This ensures that all our processes, from the receipt of raw materials to the release of the final product, meet the highest quality and safety standards. In addition, we implement a quality management system that includes process validation, change control and regular internal audits.

We can adapt our manufacturing and packaging processes to meet the specific requirements of each client, including pilot batch production, formulation adjustments, and customized packaging.

Our facilities include certified stability chambers simulating all climatic zones, enabling both accelerated and long-term stability studies in compliance with ICH guidelines.
This ensures our products maintain their quality and efficacy throughout their entire shelf life.