Get in touch. Help and support. Study and learn technical writing at both basic and advanced levels. If the company complies, they will receive their PEFC chain of custody certificate. The Society produces multiple live, one-hour, webinars each month on technical communication topics ranging from accessibility to user experience design. Building code. Technical Writing: Documentation on Software Projects By Amber Israelsen Whether you need to document requirements, architecture/design, code, test plans, or manuals for end users, this course gives you tips and best practices to do it all. Technical Documentation for Non-Writers This instructor-led, live training (onsite or remote) is aimed at persons who wish to write technical documentation but lack the experience of a trained technic... Thailand +63 9176514349 thailand@nobleprog.com Message Us. If the certificate is given for the party of the products, its term is unlimited. Document creation ; Project management ; Technical Writing Graduate Certificate. Certification; CASCO; The ISO Survey; Resources; SDGs; About us. As a manufacturer, it is your responsibility to draw up the EU declaration of conformity(DoC). as listed in Annex I) of the IVDD. The technical documentation can play a vital role in protecting a company, as it will retain information on how the product was developed and how it has evolved during the production run, along with provide evidence of the efforts undertaken to ensure the product remains compliant. In engineering, technical documentation refers to any type of documentation that describes handling, functionality and architecture of a technical product or a product under development or use. Export Certification Label: An official document or label issued by the NPPO for use by an Authorized Facility in lieu of a phytosanitary certificate. 01.110 Technical product documentation Including rules for preparation of user guides, manuals, product specifications, etc. This is the first in a series of courses for technical writers who want to learn how to write API documentation. Study and learn technical writing at both basic and advanced levels. The home for Microsoft documentation and learning for developers and technology professionals. The term technical documentation (or technical file) refers to all the documents that a medical device manufacturer has to submit. By the end of this training, participants will be able to: Produce technical content that's accurate and user-friendly. Expertise … Canada United States Europe. Students who searched for technical writer certification found the links, articles, and information on this page helpful. BSI has a strong commitment to providing the most experienced and efficient routes to market. The Technical File must be available as soon as the product is placed on the European market, whatever its geographical origin is. If the company complies, they will receive their PEFC chain of custody certificate. Advanced Certificate Course in Structured Writing for Technical Documentation (30 Hours) Technical Communication Industry Certificate- Mastery Level (160 Hours) Certificate in Professional Technical Communication (140 Hours) Mozilla Open Badges. The Certificate of Conformity to Technical Regulation may be given only by an authorized organ in the sphere of certification. Let's get this conversation started. The intended recipient for product technical documentation is both the (proficient) end user as well as the administrator / service or maintenance technician. My VMware; Partner Connect; Support . To achieve the Certified Professional Technical Communicator (CPTC) – Foundational designation, applicants demonstrate knowledge and understanding of best practices in technical communication by passing a test. A significant stage of the CE marking process is to produce technical documentation for the product to provide evidence of conformity for the relevant legislation. Online technical training for career-minded individuals, corporate employees, military, government, current technical writers and consultants. FSC Certification Certification FSC. The Foundation Certification focuses on knowledge of the field. Home; About us. Get in touch with specialised assistance services, Get advice on EU rules that apply to your business / solve problems with a public authority, Licensing and selling intellectual property, Infringement of intellectual property rights, Taxes on parent companies and subsidiaries, Request a review of a public procurement procedure, E-commerce, distance and off-premises selling, Package travel and linked travel arrangements, Technical documentation and EU declaration of conformity, Classification, labelling and packaging of chemicals, conformity assessment for protective equipment, conformity assessment for 3D printing and 3D printed products to be used in a medical context, applicable legislation for leave-on hand cleaners and hand disinfectants (gel, solution), national contact points for medical devices, EN 149:2009 Respiratory protective devices – Filtering half masks to protect against particles - Requirements, testing, marking (commonly referred to as 'FFP masks'), EN 14683:2019 EN Medical face masks - Requirements and test method, EN 166:2001 Personal eye-protection – Specifications, EN 14126:2003 Protective clothing - Performance requirements and tests methods for protective clothing against infective agents, EN 14605:2009 Protective clothing against liquid chemicals - performance requirements for clothing with liquid-tight (Type 3) or spray-tight (Type 4) connections, including items providing protection to parts of the body only, EN 13795-1:2019 Surgical clothing and drapes - Requirements and test methods - Part 1: Surgical drapes and gowns, EN 13795-2:2019 Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - Part 2: Test methods, EN 455-1:2000 Medical gloves for single use - Part 1: Requirements and testing for freedom from holes (MDD), EN 455-2:2015 Medical gloves for single use - Part 2: Requirements and testing for physical properties (MMD), EN 455-3:2015 Medical gloves for single use - Part 3: Requirements and testing for biological evaluation (MDD), EN 455-4:2009 EN Medical gloves for single use - Part 4: Requirements and testing for shelf life determination (MDD), EN ISO 374-5:2017 Protective gloves against dangerous chemicals and micro-organisms - Part 5: Terminology and performance requirements for micro-organisms risks, EN ISO 13688:2013 Protective clothing - General requirements, EN ISO 10993-1:2009 Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process, The ‘Blue Guide’ on the implementation of EU products rules, Publications Office of the European Union, ensure the technical documentation is made available to the market surveillance authorities (should they request to see it), keep the technical documentation for 10 years, your name and address, or those of any authorised representatives, identification of the product, for example, the product's serial number, the name(s) and address(es) of the facilities involved in the design and manufacture of the product, a statement of relevant regulations to which the product complies, identification of technical standards with which compliance is claimed, your name and full business address or that of your authorised representative, the product's serial number, model or type identification, a statement, stating you take full responsibility, means of identification of product allowing traceability – this can include an image, the details of the notified body which carried out the, the relevant legislation with which the product complies, as well as any, supplementary information (if applicable). About Medcert; Our history; Our services; Our ... Home > Product Documentation (Technical File) – example. Such as information deemed to contribute to the proof of the conformity of the product that is not listed in the directive. Green Certification. So why do they operate in silos? 1. Successfully conveying complicated content to end users — both internal and external — is vital and can greatly enhance the value of products and services. All European CE-marking directives and regulations oblige the non-food product manufacturers to prepare technical documentation, also known as “Technical File”, before providing the final Declaration of Conformity. The document may be given for the period of 1, 2 or 3 years in the case of series production. The Society for Technical Communication is the world’s largest and oldest professional association dedicated to the advancement of the field of technical communication. Technical Writing One and Technical Writing Two consist of two parts: pre-class lessons; in-class lessons with a facilitator and other students; The pre-class lessons provide a solid educational experience, which the in-class lessons enhance. Information on CE Technical File - documents for CE Mark certification is covered in CE Mark total documentation package, provided with free DEMO by Global Manager Group. ... Watch live and recorded events. Special Offers Course Types Course Catalogue Partnerships and Certifications Training FAQ OMG Certifications … The file must be made available to the competent authorities of the member states for at least ten years after the date that the product was last manufactured. Product(s) Building code. BSI offers technical documentation review through our CE-Excellence services; you will be assigned a dedicated Scheme Manager to work with you throughout your product certification journey and will remain your point of contact thereafter. 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