Products

PharmOut offers software products designed specifically for regulated industries, especially customised for the Pharmaceutical, Medical Device and Biotechnology manufacturers.

Quality Management Systems

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, it is an extremely cost effective suite of software..

we can assist you and great reduce your development time.

Electronic Documentation Management Software (EDMS)

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.

Professional Experience

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.

ISO 9001:2000 Quality Management Systems

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.

ISO 13485:2003 Quality Management Systems

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.

FDA's QSR 820 Quality Management Systems

PharmOut offers a FDA QSR 820 Quality Management System for Medical Device Manufacturers who manufacture Medical Devices for the USA and FDA regulated markets.

 

 
Validation Master Plans

 

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