Iberfar

Certifications

Our manufacturing facility is a symbol of trust and quality. Inspected and approved by Infarmed, it fully complies with European Union Good Manufacturing Practice (GMP) standards, ensuring safe processes and products of the highest quality.

We hold the international certifications ISO 14001 and ISO 45001, reflecting our commitment to environmental sustainability and to safeguarding the health and safety of our employees.

We are authorised to manufacture non-sterile solid and liquid dosage forms, including psychotropic substances, meeting the most demanding market requirements.

In addition, we are qualified to carry out secondary packaging of medical devices and to certify batches of sterile products originating from EU countries – providing a comprehensive service with high quality standards and regulatory compliance.

WE ARE COMMITTED

TO QUALITY

cGMP compliance

WE CARE

ABOUT THE ENVIRONMENT

ISO 14001:2015

WE ARE COMMITTED

TO PEOPLE’S HEALTH AND SAFETY

ISO 45001:2018

Capacities

Our manufacturing facility is equipped with robust and versatile production capabilities, allowing us to efficiently meet the diverse needs of our clients. Our production lines are prepared for industrial-scale volumes in the following categories:

2.000 M units

30 M units

40 M units

(average value considered for the calculation: 20 tabs/caps per package)

10.6 M units

(average volume considered for the calculation: 100 ml flask)

29.4 M units

(average volume considered for the calculation: 15 ml sachet)

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