Technology can be a game-changer that streamlines complex processes, enhances productivity and increases efficiency. For Life Sciences organizations, a structured component authoring (SCA) platform can help transform the medical authoring and documentation process — as long as you can get everyone on board. With this in mind, we’re sharing our top three tips for a successful SCA implementation.
In the Life Sciences industry, anything that can help keep your organization agile in the face of regulatory change is essential. Content development and publication decisions should be easy to make, leaving you free to focus on more important things. If you know what to look for, a structured component authoring solution can help.
Reliable, compliant documentation is essential, but creating, reviewing, and publishing that content takes time and human resources. With Docuvera’s intuitive SCA solution, your organization can reap the benefits of a cloud-based documentation system designed exclusively for Life Sciences.
On the surface, structured component authoring (SCA) is a concept that makes sense in theory but has been hard to implement for many organizations. Much of the medical authoring and documentation done today is accomplished through standard desktop publishing programs like Microsoft Word — but these programs are not designed with Life Sciences authors in mind.
Imagine this: you’re working on groundbreaking innovations for the Life Sciences industry. Your team is composed of multiple people with various specialties, spread across time zones (and sometimes, continents). There are clinical trials, endless regulatory and ethics requirements, and countless changes to critical documentation in the authoring process. You might be on the cusp of changing the world — yet you’re using Microsoft Word to manage and publish your information.
Docuvera’s easy-to-use SCA solution leverages the cloud to provide a streamlined, transparent documentation process that can transform business.
Break free from outdated methods in pharmaceutical documentation. Docuvera’s Structured Component Authoring revolutionizes processes efficiently.
With Docuvera and Structured Component Authoring reduce document creation time, increase output, and improve your bottom line without adding staff.
Transform Life Sciences documentation with Structured Component Authoring and streamline workflows, reduce errors and enhance compliance.
With cloud-powered SCA revolutionize how you create, review, and publish life science documentation and content
Introducing Docuvera – Software to create Life Science documentation that lowers cost and increases compliance
Pharmaceutical company Boehringer Ingelheim selects Docuvera to enable medical authors to efficiently build clinical and regulatory documents from pre-approved components of medical content.
Explore Eli Lilly’s Global Medical Information journey: From Traditional to Component Authoring. Change Leader Cecil Lee examines four milestones in their adaptive content creation journey.
Explore Eli Lilly’s Global Medical Information journey: From Traditional to Component Authoring. IT lead Allan Kirui examines how to set up the right environment for success, from preparation through to deployment and service management.
Explore the capabilities of Docuvera: Webinar video featuring how Notifications and Tasks in Docuvera simplify project tasks and keep users informed through seamless content updates
Explore the capabilities of Docuvera: Webinar video featuring how the simple and efficient documentation review and approval processes function in Docuvera.
Explore the capabilities of Docuvera: Webinar video featuring an overview of how you can save time and achieve consistency in your documentation by standardizing your templates in Docuvera.
Explore the capabilities of Docuvera: Webinar video introducing how component authoring works within Docuvera.
Download this Docuvera data sheet to learn how to optimize the creation and maintenance of Quality Documents/SOPs in pharmaceuticals.
Download this data sheet to learn how Docuvera enhances efficiency in creating and updating documents for Aggregate Reporting and Safety Writing.
Download this data sheet to learn how Docuvera enables efficient authoring and updates to CMC documentation throughout every step of the pharmaceutical manufacturing process.
Download the data sheet to see how using Docuvera’s component authoring approach of authoring, reviewing and updating discrete blocks of content only once, the creation of medical letters can be improved.
See in our data sheet how Docuvera simplifies and improves the efficiency of creating and updating labeling & regulatory documents by reusing approved content.
Download the datasheet for insights on how Docuvera enables you to: Streamline clinical document efficiency & Reduce author burden through content reuse.
This video will introduce you to the concept of structured component authoring and Docuvera.
See how Docuvera’s intuitive web interface streamlines compliant document creation in just 5 minutes.
A thought-leading webinar on how to prepare your business to take advantage of reusable component authoring.
