In the pharmaceutical industry, strict standards exist to ensure the safe consumption and manufacture of drugs. Every pharmaceutical product is made according to a set of directions listed in a specific pharmacopoeia published by one of several countries. Boepharma provide all pharmaceutical products according to the most up to date pharmacopoeia for all products.
When the pharmaceutical Monograph is unavailable, the standard used by the manufacturer will be substituted when appropriate.
Tests are conducted in accordance with internationally approved and lastest version of standards such as EP, BP, USP as well as DIN, EN and ISO.
Boepharma play as independent party on analytical tests to help ensure all pharmaceutical and medical devices,healthcare products meet their respective pharmacopoeia standards.
Boepharma also have cooperation with many well known analytical company like SGS, CTI, etc.
Boepharma only provides products from facilities that have met the WHO and local GMP requirements.
Our Quality Control (QC) system supports everyday activities related to the correct production, packing and internal control and release of products, all of which must be carried out prior to the release of delivery.
Our requirements pertaining to the quality control of our pharmaceutical products have one goal: to serve the health needs and welfare of the end consumer. Such far-reaching social responsibility imposes equally important moral obligations on us to market drugs of continuing uniformity and safety. Our clients can be rest-assured that they are providing their clients with quality products.
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