VALENCIA

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 Valencia

Farmalider MFG Plant Valencia specializes in the manufacturing, handling, and packaging of pharmaceutical products, food supplements, and nutritional and dietary products.

Liquid Dosage Forms:

Oral suspensions, Oral solutions

Solid Dosage Forms:

Soft gelatin capsules, Hard gelatin capsules, Oral powders, Orodispersible granules, Granules for oral solution

Packaging formats:

Sobre

Sachets

Icono sticks

Sticks

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

  • Clean rooms
  • Microbiology and physicochemical laboratory
  • Climate-controlled warehouse
  • Specialized equipment for solid and liquid dosage forms
  • Packaging lines for sticks, sachets, blisters, and bottles
  • Serialization lines


Farmalider has made a significant investment in acquiring this new manufacturing plant and in specialized equipment to ensure proper production and reliable supply to our clients and partners.

Stick Pack Manufacturing Lines:

  • 1 solid line: oral powders and orodispersible granules
  • 1 liquid line: oral solutions and suspensions

Advantages of Stick Pack Format:

  • Easy to use and administer (accurate dose, suitable for children and adults, convenient to transport)
  • Safe, aseptic, and disposable presentation
  • Ideal for OTC medicines and single-dose supplements

Certifications

Complies with the principles and guidelines of Good Manufacturing Practices (GMP). The facility is GMP-certified by the Spanish and International Health Authorities and has been audited and approved by 32 national and international pharmaceutical companies.

Production capacity

0

m2

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0
million packs/year
Total production capacity
0
stick-pack
production lines
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Exports to over 15 countries
with more than 4 million stick-pack boxes per 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.