“MOLEN PHARMA”, a Dutch company, specializes in manufacturing and selling High quality veterinary pharmaceutical products and nutritional supplements at affordable prices. Our products are distributed to farmers worldwide, ensuring the health and welfare of both animals and farmers.
Operating from our facilities in Molendijk, located in The Netherlands, we adhere to European GMP and GMP+ Guidelines during the production of veterinary medicines, feed additives, and premixes. Our commitment to quality includes customized labeling and proper registration of each product, complying with national regulations.
All MOLEN PHARMA products are manufactured within the EU and undergo rigorous quality checks by the strict Authority. Our qualified person (QP) ensures their safety and effectiveness before releasing them to the market.
Our registration department collaborates closely with distributors, providing technical and quality dossiers for product registration in various countries. At MOLEN PHARMA, we prioritize sustainable, trustworthy, and long-term partnerships with our global distributors.”
” MOLEN PHARMA “founded on 1ST JANUARY, 2018, in Molendijk, the Netherlands, is committed to delivering top-quality animal health products to customers worldwide. Our GMP-manufactured products are exported globally, supported by a dedicated team of scientists, nutritionists, and sales professionals.
From its modest beginnings in the Netherlands, MOLEN PHARMA now supplies veterinary products—ranging from medicines to feed additives and disinfectants—to partners across Europe, Asia, Africa, and the Middle East.
is to provide high-quality products at reasonable prices, ensuring the well-being of both animals and their owners. To achieve this, our veterinary products adhere to cG.M.P. regulations, while feed additives comply with G.M.P.+ standards. Regular inspections by authorities result in full G.M.P. approval.
At MOLEN PHARMA, continuous research and development drive product improvement, safeguarding animal health. Our employees mirror our commitment to reliability, ensuring efficient customer service and clear communication with partners worldwide.
We recognize that knowledge is key to prevention. Beyond medicines, we offer feed additives to proactively maintain animal health.
Integrated Innovation
We strive to create integrated solutions and innovative ideas that revolutionize animal production and care. Our focus is on minimizing environmental impact, simplifying processes, and enhancing efficiency.
Engage and Collaborate
We think beyond boundaries within the animal health domain. By involving, connecting, and collaborating with our clients, partners, and community, we drive transformation and evolution in the sector.
Building and Nourishing Relationships
We establish open and transparent channels to inspire, invest, connect, collaborate, and conduct business. Together, we grow and thrive.
collaborative efforts between us and major factories that manufacture veterinary drugs. These factories hold ISO certifications and comply with the European Union Good Manufacturing Practice (EUGMP) standards. Let’s dive into the details:
Collaborative Manufacturing of Veterinary Drugs: ISO and EUGMP Certification
- ISO Certifications:
- ISO (International Organization for Standardization) certifications ensure that manufacturing processes meet global quality standards.
- These certifications cover various aspects, including management systems, product quality, and safety.
- Collaborating with ISO-certified factories ensures consistent quality and adherence to best practices.
- EUGMP Standards:
- EUGMP refers to the minimum standards for medicines manufacturing within the European Union.
- Compliance with EUGMP is essential for any manufacturer intending to supply the EU market.
- EUGMP requirements focus on product quality, safety, and consistency.
- Benefits of Collaboration:
- Quality Assurance: Collaborating with ISO and EUGMP-certified factories ensures high-quality veterinary drugs.
- Efficiency: Shared inspection reports and information streamline oversight processes.
- Risk Mitigation: By leveraging each other’s resources, regulators can focus on areas with higher risk.