Medical Devices Directives (93/42/EEC) and Technical File Preparation Workshop
30/05/13 - 31/05/13
The workshop was held for two days aiming familiarize delegates with the requirements of Directive 93/42/EEC as amended by Directive 2007/47/EEC. The training was designed for quality and regulatory professionals in their field with the technical documentation requirements of the Medical Device Directive 93/42/EEC, which includes the 2007/47 amendment. The event was organized by Singapore Manufacturer’s Federation, in collaboration with DH RegSys Pte Ltd and SGS International Certification Services Singapore Pte Ltd. Ms Tan Hwee Ee and Ms Lee Lai Mei were the key trainers for this workshop.