an independent sounding board, testing and validating the latest thinking, and uncovering industry insight to develop compelling yet pragmatic strategies to provide business value and meet the needs of patients, payers, and prescribers. Today, we host 10 such forums across the spectrum of Pharmacovigilance, Regulatory Affairs, and Clinical Research. With over 120 member companies, our network forums are vibrant communities which foster innovation and accelerate growth. Our annual benchmark provides members with the opportunity to understand and improve their performance; and enriches our organization with unique and deep industry insights. The insights derived from our networks feed into our services and enable us to develop industry specific IPs that keep us at the leading edge of the industry. Our clients benefit from these rich insights, both in terms of cost and quality. We invest in the future of the industry, with technologies and services that enable our clients to meet the challenges of tomorrow, today. We have always believed in investing in the right technology, and our constant endeavor to strengthen our technical capabilities has helped us maintain business continuity during the pandemic. We are proud to have conducted multiple COVID-19 clinical trials as well as non-COVID clinical trials by leveraging our technology IPs. We hold 8 Life Sciences focused technologies that have been developed to meet the unique needs of the industry and provide a single source of truth. Our unique technologies developed for Regulatory Affairs and Pharmacovigilance enable organizations to be compliant with the latest regulatory requirements. Our products include: pharmaREADY®, traceREADY, idmpREADY, labelREADY, rimREADY, safetyREADY, and affiliateREADY each addressing a unique need of the industry, bringing in efficiency and reducing cost. OneClinical® Analytics, our Artificial Intelligence (AI) driven platform, enables virtual clinical trials to run efficiently. Our innovative Regulatory Technology, pharmaREADY®, achieved 200 active customers driving accelerated compliance and delivering first-time-right submissions. With regulatory requirements having evolved, becoming more complex, costly, and global in scope life sciences companies are being forced to compete, innovate, and execute faster than ever before. First launched in 2005, pharmaREADY® is a fully integrated, regulatory compliant, web-based platform to create, view, and manage global regulatory submissions. We continue to evolve our technology to ensure a robust product suite with multiple modules including: Document Management System (DMS), electronic Common Technical Document (eCTD), Structured Product Labeling (SPL), and Training Records Management System (TRMS), to meet global regulatory requirements. "Our clinical facilities comply with the International Council of Harmonization ­ Good Clinical Practices (ICH-GCP). Our laboratories are certified by the College of American Pathologists' Laboratory Accreditation Program and are also ISO 15189:2012 (Medical Laboratories ­ Requirements for " We hold 8 Life Sciences focused technologies that have been developed to meet the unique needs of the industry and provide a single source of truth. The unique technologies developed for Regulatory Affairs and Pharmacovigilance enable organizations to be compliant with the latest regulatory requirements "
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