Our story begins during the Second Industrial Revolution, when Frederick E. Zuellig established a Drug Department in the Philippines in 1938, specializing in the trade, marketing, and distribution of healthcare products.
After the Second World War, the founder’s two sons, Dr. Stephen and Gilbert diversified the business and went beyond the traditional trading activities and added the contract manufacturing services where Pharmaceutical Industries (Pharma Industries) was founded in 1953.
In 1974, contract manufacturing services for local and multinational pharmaceutical companies continued to grow, and with a desire to offer more, the Zuellig-owned Pharma Industries merged with Muller and Phipps of the United States to establish Interphil Laboratories, Inc.
Interphil has been an integral part of the Pharma Industries Group for many years. Pharma Industries is the largest pharmaceutical contract manufacturer in South East Asia, producing more than 400 formulations for more than 40 multinational pharmaceutical companies and exporting across the globe.
Pharma Industries, Inc. and Muller and Phipps Manufacturing Corp. pioneered the contract manufacturing business concept in the Philippines.
Pharma Industries and Muller and Phipps production facilities were integrated into a single compound in Sucat, Muntinlupa forming Interphil Laboratories, Inc.
Expansion of Interphil’s Sucat, Muntinlupa Plant for new Warehouse, QC Laboratory and Beta-Lactam production facilities.
Business expansion to non-pharmaceutical products such as baby care, personal health care as well as animal feed supplements.
The new Canlubang plant in Laguna, Philippines has broken ground to meet the current stricter GMP requirements.
Dr. Stephen Zuellig welcomes Pres. Fidel V. Ramos at the inauguration and commercial operation of the most modern pharmaceutical manufacturing plant in Southeast Asia.
Obtained full ISO 9001 certification, gained approval from the Australian Therapeutic Goods Administration and installed the first softgel capsule facility.
Expansion of services to Planning and Procurement of materials and the first export shipment to Taiwan.
Transfer of Cephalosporin and Penicillin facility to Interphil Plant 2, the former Novartis plant in Canlubang, Laguna.
Production System upgrade from Materials Resource Planning (MRP) to Manufacturing Resource Planning (MRP2).
Implementation of the Enterprise Resource Planning SAP/ERP integrated system having a unified view of the enterprise resources.
Expansion of services by launching the Product Licensing business, gaining additional market partners and contribution to the healthcare industry.
Started production of cosmetics, topical products and personal care products.
Gained certifications from the Republic of China Food and Drug Administration (Taiwan FDA) for safety and quality of food, drug, medical services and cosmetics.
A well maintained manufacturing facilities which is kept at par with the generally acceptable standards.
To be the strategic and progressive global partner in the healthcare industry, propelled by quality - driven operational synergies and competencies nurtured in an energized workplace.
Our Core Values
We at INTERPHIL LABORATORIES commit to live the organization's core values. Practicing and integrating those core values in our daily professional and personal lives enable us to attain our purpose.
The uncompromising adherence to a code of moral and ethical standards characterized by utter sincerity, honesty and candor
Achieving greater results by working together, enhancing individual effectiveness
Our competitive advantage, the cornerstone of all our activities.
"Discipline" is consistent and voluntary adherence to prescribed codes, systems, policies, rules and regulations to strengthen the character of the organization and its employees
"Solicitude", a deep regard and concern for the company, its employees, the community and the environment
The genuine desire to provide exceptional "service" to all stakeholders
We are accredited and certified by Philippine FDA, TGA Australia, Taiwan FDA and ISO 9001:2015 and strictly follow worldwide acceptable standards of Pharmaceutical Inspection Co-Operation Scheme (PIC/S) GMP.
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