Join us in March 2022 to learn from the best in the drug development industry and have an opportunity to learn from their experiences.
With an agenda covering the future of Clinical trials and drug development post COVID, Clinical Trials Innovation Programme 2022 will feature tailored sessions presented by the leading experts from across the globe.
We are bringing together the best in the industry to help you learn and grow, and accelerate your drug development journey.
THE TRIALS OF THE FUTURE
BOOSTING TRIAL DIVERSITY
USE OF RWD & E
CLINICAL TRIALS SUPPLY CHAIN
PAVING THE WAY FOR DIGITALIZATION
PATIENT ENROLLMENT & RETENTION
European Cancer Patient Coalition
VP, Clinical Development Operations
Head of Clinical Trials
Medical Products Agency
Meet our professonals
Managing Director & VP of Operations
Head of Global Clinical Development & Operations Patient & Site Engagement
Vice President of Strategy, MyVeeva for Patients
European Cancer Patient Coalition
Lead Data Processing Solutions
The Janssen Pharmaceutical Companies of Johnson & Johnson
Danish Medicines Agency
General Manager, Digital Measurement Solutions
Head of Clinical Trials
Medical Products Agency
Global Clinical Development TA Lead Nephrology and Orphan Disease Area
Clinical Trial Management | Artificial Intelligence | AI Speaker
Senior Operation Data Manager
Principal Data Manager
VP Clinical and Regulation
what people say
Get yours why they are still available
CATO SMS is a global provider of clinical research solutions, including strategic consulting, full-service clinical trial operations, biometrics and clinical pharmacology. With more than 30 years of experience focusing on the needs of small and midsize biopharmaceutical companies, CATO SMS effectively designs and executes studies — from strategy to approval — in complex indications and modalities across a variety of therapeutic areas with a proven center of excellence in oncology. CATO SMS’ regulatory, therapeutic and operational expertise enables the company to meet goals and exceed expectations.
Biomax Informatics provides services and software solutions for efficient decision making and knowledge management at the intersection of life sciences, healthcare and information technologies. With their neuroimaging solution NICARA they provide better outcomes from neurodegeneration clinical trials delivering the most precise brain image assessment. NICARA for clinical trials allows you to:
NICARA helps everyone working with brain data to explore the world of Connect omics in combination with Morphometry. Biomax has more than 20 years expertise and is certified according to ISO 9001 and 27001.
Lumis Life Science Consulting GmbH was founded in 2020 as a subsidiary of Lumis International GmbH with the focus to provide consulting to small and mid-sized medical device and biopharmaceutical companies when outsourcing their clinical activities. Their services cover the whole spectrum of vendor selection and management, clinical trial oversight management and training. Supporting the growth of their clients, they analyse and establish complete quality management systems to enhance their inspection readiness. Jointly with their customers, they develop tailored solutions to optimise their clinical product development programs. they collaborate with a network of experienced subject matter experts, cooperation partners and consultants for the best services in the different areas. Flexibility and empathy are core to the Lumis brand. They go the extra mile to support their clients.
For over 30 years, METRONOMIA has been an exceptional Data Science CRO partner for biostatistical, clinical data management and medical writing services. Their team of 95 highly skilled and committed employees has delivered over 600 successfully conducted projects in all clinical development phases and major therapeutic areas with the highest degree of flexibility, reliability and quality.Our Unique Selling Points:
Established in 2011, BAP Pharma is the fastest-growing, independently owned clinical trial supply organisation, with specialist divisions in Comparator Sourcing and Secondary Packaging and Labelling.They are a global leader in the clinical trial supply industry, through their expertise, innovation and dedication to providing exceptional value and unrivaled customer service.
BAP Pharma focuses on ensuring the whole clinical trial supply process is proactively and expertly managed, utilising quality assured partners, to ensure products arrive in the right condition.They offer bespoke access solutions to their clients through their unrivaled customer centric approach, to provide truly innovative solutions, to meet the complex supply challenges that pharmaceutical and biotechnology companies face.
The Almac Group is an established contract development and manufacturing organisation providing an extensive range of integrated services across the drug development lifecycle to the pharmaceutical and biotech sectors globally. Their innovative services range from R&D, biomarker discovery, development and commercialisation, API manufacture, formulation development, clinical trial supply, IRT (IVRS/IWRS) through to commercial-scale manufacture. The international company is a privately owned organisation that has grown organically over the past five decades now employing over 6,000 highly skilled personnel across 19 facilities including Europe, the US and Asia.
Since 1997, Clinigen Clinical Supplies Management has offered a dynamic range of fully integrated services to meet the complex clinical supply challenges pharmaceutical and biotechnology companies face. Part of the Clinigen Group’s global supply chain facility and depot network, it combines market-leading clinical trial services such as comparator sourcing, packaging and labelling with biological sample management. Clinigen Clinical Supplies Management delivers tailored solutions for clients to ensure their clinical trials are a success, regardless of size or scope, from Phase I to Phase IV projects.
Veeva is the global leader in cloud software for the life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 1,000 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs. As a Public Benefit Corporation, Veeva is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves.
CRYOPDP is the first choice courier for the Life Sciences and Healthcare industries with more than 25 years of experience, which has a mission to improve the health of people around the world. Headquartered in Paris, France, CRYOPDP provides turnkey premium temperature-controlled logistics solutions to the Clinical Research, Pharmaceutical, and Cell and Gene Therapy markets.
The company covers a significant portion of the healthcare temperature-controlled supply chain, including premium services, packaging, pick-pack kit preparation, specialty courier support, and premium added value solutions such as Lab Move, Direct-to-Patient, and Control Tower, a fully integrated project management solution.
Emtex Life Science, founded in 2001, is an independent and compact company that offers professional medical writing & related services. Worldwide, over 50 companies have relied successfully on their professional services.
Their professional knowledge (over 20 years of experience) and scientific background allow to provide high quality services, freeing your time and resources. Over the years, they have built specific knowledge in multiple therapeutic domains. They have provided medical writing and related services in various specialty topics including, but not limited to, preclinical, clinical, pharmacokinetics, pharmacodynamics, and quality of life. All of their team members receive ongoing, intensive (internal and external) training to deliver excellent services. Discover the advantages of working with them.
MEDizzy is the world’s fastest growing medical learning community. Together with our network of partners we educate over 10 million now and future healthcare professionals.We provide an innovative technology designed to enable quick and easy access to the latest medical knowledge. We offer a unique medical learning experience appreciated by HCPs from over 120 countries.
The Pharma Times provides with the latest breaking news and videos straight from the Pharma industry including in depth coverage, news, views, reviews market dynamics, research and design of this industry. We assure you of our best services in covering all the news, reports & press releases for pre & post events.
Exhibitors Voice is a platform that caters to all your service requirements in the B2B sector. You can rely on us to gather a good number of potential clients. In today's era, creating a digital impact is necessary. They have updated news, information, and opinions on the entire B2B segment through valuable contributions from individuals and corporations. The site is a valuable resource for multiple B2B requirements. They strive to serve the target audience's needs worldwide by giving a one- stop solution for resources from multiple industries. Your worthy contributions are given due credit and are acknowledged by advertising and content marketing opportunities. With Exhibitors Voice, you can do this in several ways, some marketing and advertising services that Exhibitors Voice provides are:
Have a look at Schedule
03 March 2022
Regulatory Experience from Advice and Assessment of Decentralised Clinical Trial Applications
Gunilla Andrew-Nielsen; Head of Clinical Trials, Medical Products Agency
Digitizing Clinical Trials – Implementing Strategies to Support Patients, Sites, and Sponsors
Tim Davis; Vice President of Strategy, MyVeeva for Patients, Veeva
Clinical Trials Innovation - AI and Decentralized Trials are the Pillars
Bhupathy Alagiriswamy; Clinical Trial Management | Artificial Intelligence | AI Speaker, Boehringer Ingelheim
Pre and Post COIVD – what has changed in the clinical research landscape?
Davy Yeung; Managing Director & VP of Operations, TCRS
Development of the Regulatory Framework for Decentralised Clinical Trials
Frederik Grell Nørgaard; Special Adviser, Danish Medicines Agency
Clinical Trials Post COVID-19: What the Clinical Trials will Look Like in 2022 and Beyond
Novel Data Streams – biosensors data in clinical trials
Giacomo Ricca; Lead Data Processing Solutions, The Janssen Pharmaceutical Companies of Johnson & Johnson
Putting the Patient First: The Significant Role of Clinical Trials Patient Engagement in the Coming Years and Insights Generation
Kimberley Kallsen; Head of Global Clinical Development & Operations Patient & Site Engagement, Boehringer Ingelheim
Digital Endpoints: The Use of Innovative Technologies to Improve Clinical Trials
Thibaud Guymard; General Manager, Digital Measurement Solutions, Biogen Digital Health, Biogen
Challenges and opportunities to conduct clinical studies in ANCA-Associated vasculitis, a rare and life-threatening disease, during and after Covid-19 pandemic’
Domenico Merante; Global Clinical Development TA Lead Nephrology and Orphan Disease Area, Vifor Pharma
The Importance of Patient Involvement in Clinical Trials and Drug Development
Antonella Cardone; Former Director, European Cancer Patient Coalition