{"id":48532,"date":"2022-09-09T16:30:18","date_gmt":"2022-09-09T16:30:18","guid":{"rendered":"https:\/\/www.arisglobal.com\/?p=48532"},"modified":"2022-09-09T16:30:18","modified_gmt":"2022-09-09T16:30:18","slug":"lifesphere-rims-product-leader-to-speak-at-raps-convergence-summit","status":"publish","type":"post","link":"https:\/\/www.arisglobal.com\/media\/press-release\/lifesphere-rims-product-leader-to-speak-at-raps-convergence-summit\/","title":{"rendered":"LifeSphere RIMS Product Leader to Speak at RAPS Convergence Summit\u00a0"},"content":{"rendered":"<p><i><span style=\"font-weight: 400;\">Life sciences veteran Laura Jones to lead a regulatory affairs session regarding investigational products at the signature industry event in Phoenix, AZ.<\/span><\/i><\/p>\n<p><b>MIAMI, FL<\/b><span style=\"font-weight: 400;\"> &#8211; September 9, 2022 &#8211; <\/span><a href=\"https:\/\/www.arisglobal.com\"><span style=\"font-weight: 400;\">ArisGlobal<\/span><\/a><span style=\"font-weight: 400;\">, the leading provider of life sciences software that automates core drug development functions with its end-to-end technology platform LifeSphere\u00ae, announces its attendance and discussion with regulatory product leadership at RAPS Convergence Summit in Phoenix, Arizona on September 11-13, 2022.\u00a0 RAPS Convergence is recognized and respected as the largest annual global, regulatory-focused event, and unites key stakeholders and decision-makers across all facets of the regulatory field for three powerful days of professional development, interactive discussion, and relationship building.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Laura Jones, Director of Product Management, RIMS, will present on Monday, September 12th. Session details are as follows:<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Title: <\/span><i><span style=\"font-weight: 400;\">How Can Regulatory Affairs Meet the Needs of Investigational Products, Scale for Future Needs, and Operate Cross-functionally?<\/span><\/i><\/p>\n<p><span style=\"font-weight: 400;\">Overview: This presentation will discuss the shifts that require Regulatory Affairs intervention in the investigational clinical study process, and how regulatory affairs can manage this process and liaise cross-departmentally efficiently. Additionally, we will discuss how Regulatory can optimize the use of a scaled-down RIM system and how organizations can scale their regulatory systems for the future as they move towards marketing a product.\u00a0 We\u2019ll dive into the regulation changes surrounding this shift and the impact they will have on current clinical trial processes and outline why a holistic approach to regulatory affairs can streamline and strengthen investigational product submissions.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Ignite! Stage Booth #337<\/span><\/p>\n<p><span style=\"font-weight: 400;\">11:15 AM \u2013 11:40 AM MST<\/span><\/p>\n<p><span style=\"font-weight: 400;\">&#8220;I am so excited to be attending RAPS this year in person, as it has been some time since being able to see my colleagues in person, \u201d shares Jones. \u201cRAPS is always a tremendous event with great conversation about where our industry is going and innovative ways to learn from each other.&#8221;<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Jones\u2019 session attendees will learn how regulatory affairs can manage investigational clinical trial registration efficiently, which regulations are causing the shift from clinical operations to regulatory affairs for investigational clinical study registrations, and how organizations can prepare for and maximize the transition from investigational products to marketed products.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400;\">ArisGlobal\u2019s LifeSphere Regulatory solutions are recognized as leading by industry analysts. The product leaders on LifeSphere\u2019s Regulatory portfolio will host a Meet the Experts breakfast networking event on Tuesday, September 13th from 7-9am at the Downtown Hyatt Regency Phoenix Convention Center.\u00a0<\/span><\/p>\n<p><b>About Laura Jones: <\/b><span style=\"font-weight: 400;\">Laura Jones is an industry veteran with 20 + years of Information Systems third-tier experience supporting a wide array of technologies concurrent with Pharmaceutical and Biotechnology Regulatory industry experience. Jones is proficient in R&amp;D technologies and implementation activities related to submission and content management, and has extensive knowledge of global agency guidance\/regulations. She has managed various system design and implementation projects for R&amp;D systems, as well as EDMS content management system integration and validation activities.<\/span><\/p>\n<p><b>About ArisGlobal: <\/b><span style=\"font-weight: 400;\">ArisGlobal is led by passionate individuals who support life sciences leaders in developing and monitoring breakthrough medicines and therapies. With more than 35 years of expertise in the life sciences industry, ArisGlobal develops technology products within the platform LifeSphere to power pharmaceutical and biotech research and development. Building on our commitment to corporate social responsibility and sustainability initiatives, we give back to the communities where we live and work \u2013 in the U.S, Europe, India, Japan, and China. For more information visit https:\/\/www.arisglobal.com\/\u00a0<\/span><\/p>\n<p><b>About LifeSphere:<\/b><span style=\"font-weight: 400;\"> LifeSphere\u00ae is the trusted partner for global pharmaceutical and biotechnology companies, health authorities, and contract research organizations. Helping accelerate product development, organize clinical trials, manage compliance, and streamline collaboration across teams, LifeSphere empowers safer, faster life science breakthroughs. As the flagship product of ArisGlobal, LifeSphere is a market-leading solution built on 40 years of industry partnership and continues to evolve in collaboration with hundreds of trusted customers. For more information visit lifesphere.arisglobal.com.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Life sciences veteran Laura Jones to lead a regulatory affairs [&hellip;]<\/p>\n","protected":false},"author":27,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[65],"tags":[],"class_list":["post-48532","post","type-post","status-publish","format-standard","hentry","category-press-release"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v23.4 (Yoast SEO v23.9) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>LifeSphere RIMS Product Leader to Speak at RAPS Convergence Summit\u00a0 | ArisGlobal<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" 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