PharmOut offers software products designed specifically for regulated industries, especially customised for the Pharmaceutical, Medical Device and Biotechnology manufacturers.
PharmOut offers an integrated suite of Microsoft® Word templates suitable for creating a Quality Management System for ISO, GMP or other regulatory compliance. Simple to use, tit is an extremely cost effective suite of software..
we can assist you and great reduce your development time.
PharmOut offers to the Asian market a local presence to assist the pharmaceutical, veterinary, biotech and medical device industries to comply with the stringent regulations of the FDA CFR 21, HSA and WHO.
With offices throughout Asia, PharmOut consultants each have many years of experience in the pharmaceutical, veterinary, biotech and medical device industries. Experience that has seen most of the problems that can occur and believe good software solutions, operated correctly can provide rapid information.
PharmOut offers a simplified ISO 9001:2000 Quality Management System for Medical Device Manufacturers who do not manufacture Medical Devices in Singapore and need a simple system.
PharmOut also offers a simplified ISO 13485:2003 Quality Management System for Medical Device Manufacturers who manufacture Medical Devices in Singapore and need the slightly more advanced system.
PharmOut offers a FDA QSR 820 Quality Management System for Medical Device Manufacturers who manufacture Medical Devices for the USA and FDA regulated markets.

