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When you need on-site attention, we’re not just here to help, we’re there to help—right by your side.
Individual courses are remarkably effective. But sometimes when you have a specific need, it helps to have expert guidance right in the room with you and your team.
In that case, we’re happy to design a custom training for your entire team, whether online—or on-site.
Learn moreRemember – at checkout you can choose to take this course On-demand. We offer a 10% group discount when you register 2 of more attendees (up to 10). Contact us for larger groups.
This 90-minute accredited training will address how to write effective Standard Operating Procedures in support of your company’s activities. You will learn how to organize and deliver information for the intended audience and purpose. You will learn how to write clear and readable documents, and how to revise and refine your own and others writing. You will learn what the necessary components of SOPs are and how to format your document according to the reader’s needs. You will learn how to develop specific patterns of SOP writing depending on who the audience is and the culture in which the audience works. This course will teach you how to effectively foreshadow upcoming events or processes within an SOP so that the reader does not skim over or miss the meat of the document.
Overall, this course is valuable because you will learn various writing techniques that will keep the reader’s attention without being redundant or adding more information than necessary. This course will enable you to create a true mental picture of the job or task at hand for the reader.
This training will benefit professionals in the pharmaceutical, medical device, biotechnology, cosmetic and food industries as well as those in other FDA regulated industries. It will be especially valuable to professionals in Quality Assurance, Engineering, Validation and Manufacturing. Directors, Managers, Technical writers and General staff charged with the responsibility for creating, reviewing, approving and implementing written standard operating procedures and instructions will find this course highly beneficial as well.
Joy McElroy
Consultant to the Pharmaceutical and Biotech Industries
Joy McElroy, has 10 years of experience as a consultant, and over 20 years total experience in the pharmaceutical and biotech industries, Ms. McElroy has gained extensive knowledge of Quality Assurance, Process and Cleaning Validation, and Equipment Qualification. She has written and executed Equipment Qualification and Validation Protocols for numerous Companies. Ms. McElroy specializes in Equipment Qualification, Sterilization, Cleaning Validation, and GMP Compliance Auditing. In 2019 Ms McElroy started her own company, McElroy Training and Consultancy. She currently works with Easi.