News & Events
December 14-15, 2015
On December 14th and 15th, i4i will be joining industry experts in Washington DC for the RIM Summit. The "Regulatory Information Management Summit" is an opportunity for industry and thought leaders to come together to explore topics and strategies that will help pharmaceutical companies learn new ways to efficiently harmonize and digitize their data and submissions. If you are going to be there, come visit i4i in the exhibit hall - Salon III, Booth 5.
November 17, 2015
IDMP is the hot topic and i4i will be there! On November 17th, the Life Sciences community will gather in Philadelphia to hear thought leaders in the industry share their insights on a variety of approaches to implement an IDMP strategy today. CBI's "IDMP Compliance and Data Management Strategy Summit" will be a full day of discussions, updates, challenges and recommendations to prepare all for a future of IDMP compliance.
October 29-30, 2015
i4i will be in Paris to present at the DIA IDMP Interactive Training Workshop, "Start Early, Finish Strong". On Friday October 30th i4i will discuss the benefits and illustrate how structured content authoring provides an environment to identify, code, extract and maintain relevant IDMP data.
October 27-29, 2015
Visit i4i at the Global Pharmaceutical Regulatory Affairs Summit in Berlin. Continuing to engage with the Life Sciences community in eSubmission and IDMP discussions, i4i is participating at the Informa Life Sciences' Global Pharmaceutical Regulatory Affairs Summit. Stop by and chat with us in the exhibition area and see how i4i's innovative structured content technology is helping clients get IDMP submission ready.
June 19, 2015
A4L 5.4 has been released! The latest version of i4i's flagship pharmaceutical solution, A4L 5.4, is ready for download.
In addition to aligning with the most current SPL Implementation and Validation guidance requirements, this latest version introduces new capabilities including support for Lot Distribution Report [LDR] SPLs, new mandatory sections required by the Pregnancy and Lactation Labeling Rule (PLLR), as well as general enhancements to the overall existing product.
For over a decade leading pharmaceutical companies have been relying on A4L to author and generate their compliant SPL submissions. Learn more about A4L here.
June 17-19, 2015
London is calling! On Thursday June 18th, i4i will present "Documents = Data" at the Marcus Evans conference; IDMP Compliance Challenge and Regulatory Information Management. i4i will share their thoughts on the value and techniques for turning your documents in the data gold source for your IDMP submissions.
This three day conference will focus on the IDMP compliance preparations in Europe, which is slated to come into force in July 2016.
April 28-30, 2015
i4i heads to Madrid. Continuing to engage with the Life Sciences community in IDMP discussions, i4i is participating at Informa Life Sciences' 5th Annual Conference on Regulatory Information Management. This year's conference wraps up with a full day focused on IDMP implementation and strategy. IDMP continues to be a hot topic for the EMA and FDA as compliance dates draw near.
April 13-15, 2015
i4i in Paris! If you are attending the 27th Annual DIA EuroMeeting from April 13-15, stop by and meet the i4i Team. We will be talking IDMP and structured authoring. Find out how your IDMP strategy can benefit from the data in your medicinal product documents. Stop by Booth 2.A12, we look forward to seeing you there!
A4L 5.4 is coming soon! Keeping up with the ever evolving SPL guidance and requirements, i4i's flagship pharmaceutical solution, A4L, will include support for Lot Distribution Reports [LDR], Wholesale Distributors and Third-Party Logistics Providers SPLs and the Human Compound Drug SPLs. In addition to the new capabilities, A4L 5.4 will include further updates to meet recent changes in the SPL guidance requirements and enhancements to the overall existing product. For licensing questions regarding existing or new capabilities please contact us at email@example.com.
February 11-13, 2015
i4i is back from Berlin after joining industry leaders for the IDMP Compliance and Regulatory Information Management conference. This event followed the 15th Annual DIA Conference on European Electronic Document Management where IDMP was the hot topic for everyone. With the July 2016 compliance date for the EU coming up quickly, it is no surprise that events are now focusing solely on the ISO IDMP standard, and how regulatory bodies and pharmaceutical companies are preparing to meet this challenge. i4i is working closely with existing and new clients to capture and manage key medicinal product information in their labeling and clinical documents for IDMP compliance. Interested in hearing more? Contact us at firstname.lastname@example.org.
Best Wishes from i4i! 2014 was a great year and it has been a pleasure helping our valued clients reach their goals over the past year. We look forward to contributing to further successes in 2015.