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Healthcare & Life Sciences ISVs TrackWise Digital by Honeywell, is the industry’s first QMS Conga equips the entire HLS ecosystem with a rich set The Quality and Safety Management solution Salesforce to leverage AI for enhancing quality related decision- of revenue lifecycle solutions, including configure, price app helps businesses manage quality and safety making capabilities. Built on the Salesforce platform it and quote (CPQ), contract lifecycle management (CLM), processes to ensure compliance with regulatory standards compromises of integrated modules that work together document automation and e-signature. Life Sciences offering deep industry solutions for Life Sciences, biotech, to support quality, compliance and more efficient and manufacturers utilise Conga to select and configure the pharma, and med devices. Use cases: audits, CAPA, effective decision making. With reporting and advanced correct products and pricing for customers, contracting, change gmt., complaints, document mgmt., management analytics across all quality processes, Life Science billing, and patient access operations. Healthcare review, safety incidents, non-conformance, risk mgmt., companies can leverage quality data to strengthen their organisations contract with providers and suppliers and supplier mgmt., inspections, training mgmt., and product culture of quality and impact company-wide performance. communicate important care information to patients and mgmt. PDM/PLM Learn More > providers. Learn More > Learn More > Cloudbyz redefines clinical trials and R&D in the Dot Compliance, established in 2015, offers the first Post Market Surveillance solution for MedTech Companies. HLS sector with a unified platform, built natively on AI-powered Quality Management System integrated into Smarteeva offers complaint handling, adverse event Salesforce. Our comprehensive suite covers Clinical Salesforce.com. It simplifies quality with ready-to-use QMS reporting, recall management, regulatoryreports and Trial Management Solutions (CTMS), eTMF, Patient and compliance processes, ensuring rapid deployment product registration tracking. 20% of MDRs (Adverse Recruitment, EDC, eConsent, ePRO, eCOA, Decentralised and cost-effectiveness. Trusted by life sciences companies Events) that go to FDA, go through Smarteeva. Trials, and Safety & Pharmacovigilance, which streamlines worldwide, it supports regulations like 21 CFR part 11 and Learn More > research, enhances collaboration, and accelerates EU-Annex 11, and ISO standards including 9001, 13485, innovation to bring therapies faster to market, ensuring 14971, and 27001. regulatory compliance and improving efficiency. Learn More > Learn More > EEMMEEA IA ISSV IV Inndduussttrry By Booookklleet — Ht — Heeaalltthhccaarre & Le & Liiffe Se Scciieenncecess 7

Salesforce ISV Industry Booklet - HLS - Page 7 Salesforce ISV Industry Booklet - HLS Page 6 Page 8

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