42
Scientific and technological services and related research; scientific and technological services relating to obtaining medical device registrations and compiling medical device registration files; Laboratory (Scientific -) services; quality control of biomedical products and medical devices for certification purposes; laboratory research and laboratory analysis; research and design for the medical industry; research and development for others; Conducting clinical trials for medical devices; consultancy with regards to clinical trial services to pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industries; quality control; consultancy on quality control with regard to pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industries; drafting and testing of quality standards, protocols, certification criteria and assessment guidelines with regard to pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industries; auditing, assessing and certifying procedures and processes; Conducting of inspections; comparative tests; automation solutions in the field of quality and inspections; auditing and provision of clinical trial services to pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industries; provision of quality management systems for pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industries; contract research organization (CRO) services, namely, monitoring of clinical trials for drugs, biologics and devices of pharmaceutical, medical, healthcare, and life sciences companies for quality control purposes; contract research organization (CRO) services, namely, clinical trial project management in the nature of design and implementation of clinical trials and quality assurance for all major therapeutic areas, including orthopedic, cardiovascular, dermatology, and aesthetics; consulting services in the field of conducting clinical trials in the pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industries; providing quality assurance services in the field of regulatory submissions to health and drug authorities by life sciences companies to ensure validity and accuracy; product development for others, namely, providing implementation services relating to the development and validation of drugs, biologics and medical devices
45
Legal services; Litigation services; Consultancy in the field of statutory rules, norms and regulations relating to clinical trials, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; regulatory compliance consulting in the pharmaceutical, medical, healthcare, and life sciences fields