Click on the name of the course to be taken to our website for class schedule, class outline, and to register. The Technical Writing class prepares you to create effective technical documents for
both written and digital media with emphasis on technical memos, problem-solving
reports, and decision-making reports.
One day class. Cost is $649.00.
Writing Policies & Procedures/SOPs
• Requirements/Guidelines for Policies and Procedures/SOPs
• Writing/Development Process & Project Reporting
• Policies and Procedures Identification and Job Task Analysis
• Writing Readable Policies
• Planning for Policies and Procedures
• Keeping the manual to a manageable/usable size
• Policy and Procedure Format and Layout
• Review and Editing Policy and Procedure Drafts
• File Naming and Storage of Policies and Procedures
• Management of Policies and Procedures
• Types of Policy and Procedure Manuals – What is needed by your organization
• Practical Practice and Writing/Drafting
Technical Writing
• Analyzing and Assessing Customer Requirements and Needs
• Identifying what readers need to know vs. what they want to know
• Technical Writing Style
• Reviewing Original Documents for Format, Sequencing/Flow & Technical Content Accuracy
• Using simple language and messaging
• Recommended Action Verbs; Using Active Voice
• Knowing the difference between technical and narrative writing
• Following the four steps of development
• Writing with greater clarity and precision
• Avoiding ambiguities
• Determining the appropriate level of detail
• Word choice and recognizing words to avoid
• Organizing material within an established format/template
• Designing pages and using visuals
• Review & Editing
• Practical Practice and Writing/Drafting
Overview:
Technical disciplines require extensive writing to a broad range of audiences, from fellow subject-matter experts concerned with methodology and processes to non-expert decision makers who are interested in cost-benefit analyses and organizational impact.
Focusing on the skills needed to write proposals, emails,
memorandum, business letters, reports, meeting minutes,
agendas, invitations and memos for maximum effect.
Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work. This webinar will help you structure your QMS and develop accurate, clear, unambiguous SOPs.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/WRITING-SOPs-501292/MARCH-2016-ES-TRAININGREGISTRY
Numerous challenges lie ahead for auditors when composing an audit report. They want to ensure that they clearly articulate a comprehensive review process, valid and reliable criteria, conditions logically linked to causes, relevant and risks, and beneficial recommendations-all with an objective style.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/AUDIT-REPORT-WRITING-501321/APRIL-2016-ES-TRAININGREGISTRY
Many candidates call the corporate career sites by their well earned nickname, Black Holes. Companies have done a great job conditioning candidates to avoid the HR processes and network around them to hiring managers because of the human resource focus on screening out candidates.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/WEBSITE-ATTRACT-NEW-TALENT-507441/SEPTEMBER-2017-ES-TRAININGREGISTRY
This training program will discuss how to effectively create performance metrics and goals for your department or project. It will also discuss the key components of a metric and when to use different types of performance metrics. The outputs of process performance and product quality monitoring are the key for continual improvement. The necessary changes can be identified, introduced, monitored and controlled to continually improve processes and systems.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/ENHANCING-CRITICAL-GMP-PROCESSES-USING-PERFORMANCE-METRICS-505933/NOVEMBER-2017-ES-TRAININGREGISTRY
This webinar will describe the elements and characteristics necessary for the development and writing of an occupational health and safety Plan. The main component of this Plan will be your 'Company Safety Manual' however, the actual Plan will encompass far more than a Manual.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/How-to-Structure-and-Write-an-Occupational-Safety-Health-Plan-506155/FEBRUARY-2018-ES-TRAININGREGISTRY
Technical Writing generally conforms to Good Documentation Practices (GDocP). This term describes standards to create and maintain documents. The term is primarily associated with the pharmaceutical and medical devices industries but applies to documents created in multiple organizations. Most companies have in-house requirements that all documents produced within the organizations conform to the firms' particular requirements. The purpose of this webinar is to define and clarify general guidelines for the creation and maintenance of documents in order to ensure consistency between documents created by various functional groups within organizations. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Technical-Writing-Best-Practices-505355/MARCH-2018-ES-TRAININGREGISTRY
This training will guide you about how to convert highly technical document into a written presentation effortlessly understood by general public. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/Technical-Writing-A-Detailed-Process-503953/MARCH-2019-ES-TRAININGREGISTRY
Outline the record retention and notification requirements for several federal laws and employers know how long to keep or destroy employee records and documents. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/Best-Practices-For-HR-Recordkeeping-Requirements-The-Question-Is-To-Keep-Or-Not-To-Keep-502592/MARCH-2019-ES-TRAININGREGISTRY
Gain insight on recent and upcoming Cal/OSHA regulatory developments and trends that will impact California employers in 2019-which is right around the corner.
Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link -
https://www.onlinecompliancepanel.com/webinar/Cal-OSHA-Update-for-2019-Hot-Spots-Practical-Compliance-Strategies-Every-Safety-Pro-Should-Know-505987/APRIL-2019-ES-TRAININGREGISTRY
If you have grammar questions and/or want editing and
proofreading for your documents ask award-winning
writer/author and popular trainer Susan Silver! Work
online or in person with her quick, Positively
Organized! methods!
Course Description - Course runs 9:00 to 5:00 both days
This course presents a comprehensive overview of the structure of American English to give non-native writers of English the tools they need to produce clear, complete, and comprehensive documents. Participants will learn about English within the context of the type of writing the therapeutic products industry requires. The course covers the structure of the language and how to control the individual components, as well as the choices writers have in delivering messages. The course also addresses specific aspects of English that are problematic for individual participants. Attendees should come prepared with specific questions they want answered during the course.
This course presents a comprehensive overview of process writing that the binding regulations require. There's a tenet among regulatory bodies: "If you didn't write it down, it didn't happen," and while the regulations tell companies what they need to do and document, they don't tell them how. Determining how systems work and how processes occur and documenting them is up to companies to assess. This course presents process writing within the "big picture" of controlled documentation and gives industry standards for delivering information. Effectively prepared process documents keep companies on track and compliant. Participants will learn how to write documents that ensure consistency in operations. A workshop in process writing gives participants the opportunity to actually write about a process and then assess the results.
The course also addresses problematic areas of the English language and affords participants the chance to voice their questions. Participants will learn . . .
Medical writing is both a science and an art. The art of medical writing is to comprehend and present scientific information clearly to suit the specific target audience's level of understanding including patients, the general public, physicians and/or regulatory agencies. Often it is not poor science that kills a scientific paper; rather, it is the lack of clarity and continuity. Poor writing can be very costly to companies and frequently slows the review process of regulatory submissions.
In this 2-day course, you will learn about the different types of medical writing and how to write effectively. We will examine various types of writing including abstracts, regulatory documents, and patient education materials. We will also consider ethical issues that face medical writers. You will gain insight into the design of effective documents and what goes into putting together a compelling manuscript. You will also learn how to keep your writing free of medical jargon and common . . .