Sponsors
3S Pharma
3S Pharmacological Consultation & Research GmbH is a CRO headquartered in Germany. Founded more than 25 years ago it performs clinical trials in Romania and Moldavia. More than 1000 clinical studies performed by 3S were registered all over the world. Clinical studies performed by 3S were inspected by EMA, by different individual European Authorities (French, German, Austrian, Danish, etc.) and, by US-FDA. In all instances the outcome was positive. 3S Pharmacological Consultation & Research also owns a bio-analytic lab specialized in HPLC-MS/MS analysis. The lab is GLP certified and was repeatedly inspected by EMA, various individual EU Authorities and by US-FDA.
ABF Pharmaceutical Services
ABF Pharmaceutical Services is a GMP-certified company with a wide range of pharmaceutical services for investigational medicinal products and approved drugs: Our services range from primary and secondary packaging including kit production and labeling, to storage and distribution at a wide range of temperatures. We take care of your product all the way through certification and release by our Qualified Persons (QPs). In addition, ABF has also established a qualified laboratory network to ensure high quality isolations of Peripheral Blood Mononuclear Cells (PBMCs).
Alcura
Alcura is a trusted global partner in Clinical supply, labelling, storage and distribution. With a focus on customized solutions, that meet the trial and patient needs. Part of Cencora family of brands. They deliver end-to-end supply chain solutions worldwide. European hub in Spain, with global logistics, packaging solutions, and clinical depot network across 38 countries. In-house solution for Advanced Therapy Medicines / Cell Gene Therapy storage & distribution, including regulatory expertise and regulatory services (MAH). Strong in comparator sourcing due to exceptional group buying power.
APICES
APICES was born in 2009, founded by a group of highly qualified professionals with a vast experience in CROs and pharmaceutical companies. They are an organization with Spanish identity and international vocation. Key employees have more than 20 years’ experience in Clinical Research fields and specialized in different disciplines which altogether provide a real and updated vision of clinical research world and new scientific development. APICES offers to customers, clinical research services to improve the quality of investigational products development optimizing the processes and activities of clinical research and market access. Delivering simplification of complex processes of clinical trials. They apply a full range of tools like field-tested technologies and with their experience and resources they are able to manage clinical trials of any size in the most efficient way.
CliniQnect
Thirty years ago, Staffan Sahlström together with Camilla Nordström pioneered the global doping control service (International Doping Tests & Management) within the sports industry by developing a system and implementing unannounced tests at athletes’ homes. In addition to this experience, they provided on-site and home collection for other industries such as maritime-, workplace and clinical trials. In 2015 they left the sport industry and co-founded First Wellness Testing AB.In December 2018, IQVIA approved First Wellness Testing to conduct Home Test Service for Clinical Trials. In order to provide a tailor-made virtual clinical trial solution for our clients, the co-founders decided to establish a new business unite “CliniQnect” – as a subsidiary to First Wellness Testing AB.CliniQnect brings all the combined expertise, experience and our broad network of qualified nurse and doctors and operation processes into the new business unite.As a company, we have been perfecting the art and science of in-home services since 1991. The depth and variety of experience among our employees and our global medical net-work will make it easier and more convenient for patients to participate in clinical studies.
Endpoint
Endpoint Clinical is an interactive response technology (IRT) systems and solutions provider that supports the life sciences industry. We deliver innovative and high-quality clinical trial management technology. Our fully customizable randomization and trial supply management (RTSM) solutions are backed by over a decade of award-winning experience and expertise. Built on client insight, collaboration and ingenuity, Endpoint RTSM solutions ensure that our clients can focus on the science of developing lifesaving medicines. With over 600 team members globally and offices across the US, EU and Asia, Endpoint is headquartered in Wakefield, Massachusetts.
IROS
Insights Research Organization & Solutions [IROS], a subsidiary of G42 Healthcare, was established in 2021 in Abu Dhabi. IROS is the first UAE-based Contract Research Organization (CRO) specializing in healthcare research, including clinical trials across all therapeutic areas, in addition to the generation and integration of real-world data. The first of its kind research organization in the entire Middle East, it provides international, ethical, and scientific quality standards in clinical trial reporting, as well as key solutions and insights that ensure access to more innovative, life-changing treatments.
NeSPaT
NeSPaT originates from the field of business travel services in 2003, so it has great expertise in organizing logistics. In 2013, NeSPaT started organizing patient travel in Ukraine. For 10 years they have been focusing only on developing of patient travel services. Now they`re a leading service of logistics in clinical trials. NeSPaT declares with full responsibility that they have transformed the benefit of patient transportation into a completely new and higher level of service.
Their basic product is an integrated solution for organizing patients’ travel and providing related services within clinical trials. The patients are provided the following services within this product:
• car transfers: in-city, intercity, and regional routes
• booking and delivery of railway, bus, and air tickets
• meal delivery
• accommodation
• relocation of patients
• delivery of biomaterial samples
• transfer of medical staff to patients
• transportation by medical transport
• transportation of Covid-19 patients
• reimbursement of patient expenses
Link2Trials
Creating the best patient experience in clinical trials extends beyond the initial start and end dates. It’s an ongoing process that begins with trial preparation and concludes with sending the trial outcome/results and a comprehensive and personalized thank you to all enrolled participants.
By taking the patient perspective (and perception) as the starting point, Link2Trails empowers you to enhance patient experience throughout the trial cycle. We can help you optimize your protocol, develop an effective e-consent process, promptly identify, recruit, and pre-select eligible participants, and provide personalized support to boost adherence.
• Patient feasibility and insight assessments
• Patient recruitment & pre-qualification
• Adherence Risk Management (ARM)
QoL Research
QoL Research is a contract research organization (CRO) who provides support to the pharmaceutical, biotechnology, and medical device industries in the form of research services outsourced on a contract basis.QoL Research provides services as preclinical research, clinical research, clinical trials management, and pharmacovigilance.This organization supports also foundations, research institutions, and universities, in addition to governmental organizations.
SCOPE International
SCOPE International is an independent Full-Service Contract Research Organization (CRO) with a network of 14 local offices and business entities throughout Europe and USA. SCOPE offers a complete range of clinical development and consulting services to the pharmaceutical, biotechnology and medical device industries, and is supported by long-established partnerships in other geographies. They’re focus on providing cost-effective services while achieving industry leading benchmarks in timelines, costs and quality. 2020 marked a significant milestone for SCOPE as they celebrated 20 years of successful business.
Science4Tech
We offer value added services underpinned by our SaaS technology and Apps to accelerate clinical trial outcomes for the sake of patients. Our data-driven solutions aim to improve all stages of clinical trials, under strict scientific rigour and in compliance with the regulatory framework.
ShareCRF
ShareCRF simplifies the complex world of clinical trials with our EDC platform that:
• It is very easy to use for both trial managers and other users.
• Enables you to collect trial data with higher quality in less time and, therefore,at a lower cost.
• Fits 97% of clinical trials like a glove, thanks to its great flexibility.
• Simplifies complex operations such as randomisation, direct participant datacapture (ePRO/eCOA), medical coding (MedDRA, WhoDRUG), trial supply stockmanagement and encryption of sensitive data.
• It makes it easy and simple to comply with regulatory requirements: FDA, EMA,GCP, GDRP, HIPAA.
Syneos Health
Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, strategically integrating clinical development, medical affairs and commercial capabilities to address modern market realities. We bring together a talented team of professionals, who work across more than 110 countries, with a deep understanding of patient and physician behaviors and market dynamics. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients.
TCRS
TCRS is a UK based, full service, international CRO that supports biopharma companies in the clinical development of their novel products. We have strong expertise in the management of a broad range of clinical trials and a network of tried and tested sites in the UK and internationally.
Wemedoo
Wemedoo is a health-tech company with a focus on clinical, medical, and real-world data interoperability. Our OOMNIA Clinical Research Information System empowers biopharmaceutical companies, clinical research organizations, academia, and hospitals to effortlessly collect, analyze, and exchange all relevant data in real-time. Our flexible and controlled data flow includes diverse sources of real-world data, which results in more efficient clinical trials with superior data quality and outcomes. Our supported SaaS business model takes care of all your data management needs and allows you to focus on your work entirely. Our solutions are tailored to your unique needs, significantly reducing clinical trials related costs and drastically shortening time to market. We are passionate about leveraging data to improve patient outcomes and committed to helping our clients achieve their research goals. Join us in revolutionizing the healthcare industry through data-driven insights.
Sponsors
To have a detailed information of different sponsorship packages kindly contact
Frank Magli
Programme Head
Email: frank.magli@pgsolx.com
Contact No: +442077892003