Programme de certification d'entrepreneurs spécialisés dans les domaines de la construction et de la rénovation d'habitations et d'immeubles résidentiels et commerciaux.

Bleaching, cleaning preparations and non-medicated cosmetics

Industrial oils, greases and fuels

Pharmaceuticals and herbicides

Common metals

Machinery

Hand tools

Electrical, scientific and teaching apparatus and software

Medical and veterinary devices

Environmental control items

Vehicles

Guns and ammunitions

Precious and semi-precious metals, and jewellery

Musical instruments

Paper and printed goods

Rubber and rubber goods

Leather and artificial leather goods

Non-metallic building materials

Furniture, mirrors, articles not included in other classes

Household goods and glass

Ropes and fibres

Yarns and threads

Textiles and textile goods

Clothing, footwear, headgear

Sewing and decorative items including slide fasteners

Floor coverings

Games, toys and playthings, sporting articles

Meats and processed foods

Staple foods

Agricultural, horticultural and forestry

Beer and non-alcoholic beverages

Wines and spirits

Smoker's articles

Advertising, marketing, promotional and business

Insurance and financial

Building construction and repair

Telecommunications

Transportation and storage

Treatment of materials

Education and entertainment

Computer and scientific

Accommodation, food and drink

Medical and veterinary, beauty, agricultural and forestry

Personal and legal

Technical writing, namely, medical writing services for developing medical protocols, clinical study reports, investigator brochures, safety reports, informed consent forms, meeting abstracts, posters, manuscripts, study charts, manuals and literature reviews; Providing access to an Internet website portal featuring clinical study and clinical trial management system tools; Electronic storage of medical images, clinical study plans, clinical study data, clinical study reports, investigator brochures, safety reports, meeting abstracts, posters, manuscripts, study charts, manuals and literature reviews, secure physical storage of electronic and paper documents; File sharing services, namely, providing access to a website featuring technology enabling users to upload and download electronic files, namely, complete and inspection-ready trial management files; Electronic storage services for archiving databases, images and other electronic data in the field of trial management files (TMF), TMF setup, archiving and management of TMP files through lifecycle of clinical study; Conducting scientific research, namely, biostatistics and statistical programming, protocol development of sample size and power calculations, randomization schedules, statistical analysis plans, statistical programming and validation in statistical analysis system, statistical analyses of clinical trial data, interpretation and reporting of data for clinical trial reports and publications, statistical and strategic consulting for product development, interim analysis for early decision-making, database integration, New Drug Application (NDA) ready data listings, regulatory submission compliant datasets, thought leadership and operational experience in the field of scientific research with study data tabulation model and analysis data models for drug regulatory submission standards, integrated safety and efficacy summaries, adaptive design consulting and simulation support, translational research support, setup and management of medical research review committees; Medical research services, namely, medical monitoring and investigator site monitoring in the field of medical review of clinical study materials, preparation of medical monitoring and safety plans, continuous trial oversight via patient level and safety data review, subject eligibility support for investigators, medical support to sites and study teams for interpretation of study protocol, consultation on potential safety issues and medical concerns and 24/7 medical monitor coverage; Pharmaceutical drug development services in the field of drug safety, specifically, processing adverse events from clinical trials, preparing Development Safety Update Reports (DSURs) and other aggregate reports, performing signal detection and benefit-risk assessments, preparing safety management plans and preparing medical monitoring plans; Providing quality assurance services in the field of clinical trials, namely, quality assistance documentation, such as Standard Operating Procedures (SOPs) and work instructions, internal system reviews, site audits, vendor assessments; Medical research services in the field of pharmacology, namely, dose simulation, selection and optimization, selection of biomarkers and endpoints, optimization of trial design, population pharmacokinetic and pharmacodynamic modeling, exposure response modeling; Medical research services in the field of translational medicine, namely, immunohistochemistry, flow cytometry, transcriptomics, proteomics, microbiome study; Providing medical and scientific research information in the field of clinical trials, namely, the design of clinical trials and outcome measures for studying human diseases, and for studying and testing drugs, devices and methods of medical treatment on humans in relation to diseases; Conducting clinical trials for others which study human diseases, and study and test drugs, devices and methods of medical treatment on humans in relation to diseases; Custom computer programming of medical imaging adjudication and computer systems integration of clinical trial subject eligibility data with Interactive Response Technology (IRT); Computer database design and implementation for data collection, data storage, data management, data analysis, and data validation for use in pharmaceutical drug development; Compilation and provision of clinical study data, namely, compiling data for research purposes in the field of medical science and medical consultancy.

Medical imaging services; Medical diagnostic testing, monitoring and reporting services; Medical imaging services, namely, electronic medical imaging support services for use in assessing patient health in clinical trials, namely, reviewing and scoring electronic medical images, including video images, of patients supplied by others; Medical imaging services, namely, histopathology support services for reviewing and scoring tissue sample images provided by others; Consulting services in the field of medical imaging, namely, magnetic resonance support services for reviewing and scoring magnetic resonance images provided by others; Medical services, namely, endoscopy support services in the field of reviewing and scoring endoscopic images provided by others.

Regulatory submission management, namely, assisting others with preparing and filing applications for new drugs with government regulatory bodies, submission planning and life cycle management of clinical trial applications to Competent Authorities, Ethics Committees and Regulatory Agencies, pre-approval submissions, submission of supplements, amendments and variations applications, submission publishing and dossier compilation in electronic common technical document or common technical document formats, annual reports, paper submissions management and submission archival.