In compliance with the International Medical Device Directive / MDD regulation, all Hospitech products are produce within the class 10K clean room environment. The establishment of clean room in Hospitech was in accordance to the international clean room standard.
Beside maintaining the stringent environmental control over the production areas, the overall process control which build by the management is also compliance to the international Good Manufacturing Practices (GMP) standard.
Throughout the years of maintaining the organization quality system management, the exposure with the SGS Yarsley International Certification Services had further confirm that Hospitech’s quality system management is conform to the International standard.
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