Aquila Solutions

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Aquila Solutions eCTD Regulatory Publishing, Consulting, and Strategy

📋 Regulatory projects involve multiple documents, contributors, deadlines, and dependencies that all need to come togeth...
10/20/2026

📋 Regulatory projects involve multiple documents, contributors, deadlines, and dependencies that all need to come together at the right time. Aquila Solutions provides project management support to help coordinate publishing activities, establish timelines, track milestones, and keep submission work moving forward. From individual sequences to larger regulatory projects, our team can provide the structure needed to keep everyone aligned. Reach out to discuss your upcoming project. 🎯

❓ Earlier than you might think. Involving your publishing team before the final deadline gives you time to set expectati...
10/15/2026

❓ Earlier than you might think. Involving your publishing team before the final deadline gives you time to set expectations, review document readiness, plan the submission structure, and identify potential publishing needs before they become last-minute issues. Aquila Solutions can work with your team ahead of delivery to help establish a smoother path toward submission-ready content. Have a regulatory milestone approaching? Reach out and start the conversation early. 📅

🎓 Strong Regulatory Operations depend on more than systems and processes. Your team also needs the knowledge to use them...
10/13/2026

🎓 Strong Regulatory Operations depend on more than systems and processes. Your team also needs the knowledge to use them effectively. Aquila Solutions provides RegOps training to help organizations strengthen internal capabilities and support consistent regulatory workflows. Whether you're developing new processes, onboarding team members, or reinforcing existing practices, experienced guidance can help you build a stronger foundation. Reach out to discuss your team's training needs. 📘

🤝 Outsourcing regulatory publishing does not have to mean handing over control of your submission. A strong publishing p...
10/08/2026

🤝 Outsourcing regulatory publishing does not have to mean handing over control of your submission. A strong publishing partner should adapt to your requirements, communicate throughout the project, and work within agreed timelines and workflows. Aquila Solutions works collaboratively with clients while managing the technical publishing activities needed to produce submission-ready deliverables. Your team stays involved while gaining additional expertise and capacity where it is needed. 🔗

📄 A finalized document is an important milestone, but it still needs work before it's ready for submission. Document pro...
10/06/2026

📄 A finalized document is an important milestone, but it still needs work before it's ready for submission. Document processing can include formatting, PDF preparation, bookmarks, hyperlinks, file organization, QC, and other publishing activities needed to prepare content for an electronic submission. Aquila Solutions can manage these details and help turn your finalized content into a compliant, organized deliverable. Reach out to see how we can support your next submission. 📂

🌎 Regulatory publishing does not stop at the FDA. Aquila Solutions supports electronic submissions across global markets...
10/01/2026

🌎 Regulatory publishing does not stop at the FDA. Aquila Solutions supports electronic submissions across global markets, including the FDA, EMA, Health Canada, MHRA, TGA, GCC, and Swissmedic. Whether your development program focuses on one market or expands internationally, our team can help you navigate the publishing requirements of each region. Reach out to learn how Aquila can support your global submission strategy. 📂

💻 SPL may be one of the better-known applications of XML in Regulatory Operations, but Aquila's XML capabilities extend ...
09/29/2026

💻 SPL may be one of the better-known applications of XML in Regulatory Operations, but Aquila's XML capabilities extend beyond a single document type. Aquila Solutions is equipped to create XML files for submission to the FDA and other regulatory authorities, supporting needs such as SPL, ACA, FAERS, and more. If your team has an XML requirement and needs experienced authoring support, reach out to discuss your project with us. 🔗

📅 Regulatory meetings require preparation well before the meeting itself. Establishing objectives, identifying key quest...
09/24/2026

📅 Regulatory meetings require preparation well before the meeting itself. Establishing objectives, identifying key questions, organizing supporting information, and allowing adequate time to develop the meeting request and package can help your team approach the interaction with a clear strategy. Aquila Solutions can support meeting requests, meeting packages, publishing, and regulatory preparation throughout the process. Reach out if you have an upcoming Health Authority meeting on your development timeline. 📝

❓ Should regulatory publishing be handled internally or outsourced? No single answer fits every organization. Aquila Sol...
09/22/2026

❓ Should regulatory publishing be handled internally or outsourced? No single answer fits every organization. Aquila Solutions can provide experienced personnel to support a client's internal publishing team and established workflows, or we can manage publishing activities using our own systems to deliver submission-ready eCTD sequences. The right approach depends on your resources, submission volume, and internal capabilities. Reach out, and we can help you determine which option makes the most sense for your team. 💬

🔹Celebrating 9 Years with Caitlin Storey!🔹Caitlin is celebrating nine years with Aquila Solutions, where she serves as a...
09/18/2026

🔹Celebrating 9 Years with Caitlin Storey!🔹

Caitlin is celebrating nine years with Aquila Solutions, where she serves as a Lead Publisher and Labeling Specialist. Over the years, her eye for detail and growing expertise have helped establish her as Aquila’s resident resource for regulatory labeling.

This year, Caitlin is taking that expertise even further. In December, she will complete the Labeling, Advertising, and Promotions Pre Master’s Certificate program at Temple University, a four-course program covering US Food and Drug Law, US and global drug labeling, and US drug advertising. Looking ahead to 2027, she plans to continue her professional development by pursuing her RAC certification.

Congratulations, Caitlin, on nine years with Aquila and on everything you continue to accomplish. We are excited to see what comes next!

Address

349 Margie Drive #100
Warner Robins, GA
31088

Opening Hours

Monday 10am - 6pm
Tuesday 10am - 6pm
Wednesday 10am - 6pm
Thursday 10am - 6pm
Friday 10am - 6pm

Telephone

+14044964171

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