We’ve come a long way from dealing with traditional paper (and paper online, i.e. PDF) documents. It’s often still needed in many cases, but in others, traditional documents are more of a hindrance than a help. To solve that problem, more companies are stepping into the word of Augmented Reality and you can as well! […]
Structured content is fast becoming today’s best practice. With the proliferation of channels and devices, we can no longer create ad hoc content and re-craft it over and over again. Structured content is content that follows a pattern, making it easy for authors to create and computers to process. It saves time, improves quality, and […]
Content is critical to regulatory approval. And, it plays a significant role between physicians and their patients, helping to teach patients how to manage medical conditions with greater independence and comply with treatment regimens. Keeping up with rapidly-changing guidelines and recommendations for patients, caregivers, and healthcare workers is difficult. Increasingly demanding requirements are putting pressure […]
Most organizations have multiple types of customers and many audiences. The standard way to deliver content is to provide all the content a customer needs and let them determine what makes sense for them. But in today’s fast-paced environment few are willing to wade through the volumes of content; be it content marketing, product content, […]
Wednesday, March 11, 2015, 1:00pm ET Most organizations have multiple types of customers and many audiences. The standard way to deliver content is to provide all the content a customer needs and let them determine what makes sense for them. But in today’s fast-paced environment few are willing to wade through the volumes of content; […]
March 16 – 10:00am PT/ 1:00pm ET The Core Data Sheet (CDS) is a critical component of the effective creation of Labeling content for different regulatory regions and outputs (Prescribing Information/Package Insert, Package Leaflet, etc.). The content is typically managed in email, complex MS Word documents, or Excel spreadsheets. It is difficult to track content […]
April 13 – 10:00am PT/ 1:00pm ET Content is produced for clinical trials, submissions, labeling, and marketing. The content is created, recreated, and recreated throughout its lifecycle. At best case it is copied and pasted into multiple documents. Often times, the original source of the content is lost within the versions. When content changes, it […]
May 4 – 10:00am PT/ 1:00pm ET Pharmaceutical companies must endure the challenges tied with global submissions. From translations to local regulatory requirements, it is difficult to maintain the integrity of Core Data Sheets and ensure consistency across submission variations. When labeling events fast-track submissions, the scramble to pull together content may result in errors, […]
If you missed Ann Rockley’s webinar Content Strategy for Adaptive Content it’s available from Mekon Ltd’s Congility website. Mekon runs the annual Congility (Content Agility) conference, and was the sponsor for the webinar. The webinar is available via this link.
If you missed Ann’s Webinar on Developing a DITA-based content strategy for reuse, it’s now available as a recording from DCL, sponsors of the webinar. You can listen to the webinar via this link. Please note that the recording includes both video and audio, so it’s a large file.