PharmOut is an international consultancy founded in 2006 which has grown a strong reputation in offering leading GMP compliance, validation, regulatory, engineering and architectural consulting services solutions to the pharmaceutical and life science industries.
PharmOut holds ISO 9001:2015 certification from LQRA and our Quality Management System is certified to the ISO 9001:2015 standard for the provision of engineering, architectural design and consultancy services.
We aim to give you a competitive advantage by helping you design, build and operate manufacturing facilities that will fully comply with international Good Manufacturing Practice (GMP) regulations as issued by regulatory agencies such as the US FDA, EU EMA, CFDA and PIC/S member agencies such as the Australian TGA, New Zealand MedSafe, Singaporean HSA to list a few of the nearly 50 agencies.
Meet some of our hugely diverse group of consultants who regularly work across the Asia Pacific Region and we can often have a GMP consultant on your door step within 24 hours
What makes PharmOut tick? What do we regard as important in our day-to-day operations, as we work for our clients, our staff and the company?
Find out what gives PharmOut the competitive edge and how we can help you.
PharmOut works with some of the world’s leading experts in specialist areas.
Learn about our customers, our services and our history.