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Vanessa Parrein

Denys Research consultants

Business Development Manager, Denys Research Consultants
After finalizing her degree in Food and Dietary sciences, Vanessa Parrein started her career in 1997 as Medical representative for P&G and BMS. In 2001 she made the transition into clinical operations and began working as a Clinical Trial Associate, first for Eli Lilly and in 2009 she joined DRC. In 2011 she promoted to Clinical Trial Manager and as of January 2017 Vanessa is the Business Development Manager for DRC. Over this 20-year period she became an expert in the set-up, the conduct and the management of Clinical Trials.

Keywords: Clinical Consultancy, Clinical Operations Management, Clinical Quality Services, Project Management, Drug/ Medical Device Development, ATMP, Audits

About Denys Research Consultants
DRC is specialized in assisting companies from market access strategy over clinical development strategy to the full setup and management of clinical trials. In parallel we offer clinical quality services ranging from audit services to the full development or optimization of quality management systems.
Our mission is adding value through a customized approach ensuring success from the very beginning in clinical research. As no two clinical development paths are ever the same, we at DRC, strongly believe in partnering with our client as of the transition from pre-clinical to clinical research. This minimizes the risk of late-stage development failures, increases the probability that optimal safety and efficacy data are available and decreases the total time involved with drug or medical device development.
Our high-quality standards and continuous investment in e-solutions, staff and training, ensures delivery within the expected timelines and an all-time inspection readiness. Our personal approach is key in our believe that we are not just a service provider but a trusted partner for the long-run. Our services:

Consultancy
• Optimization of TPP / Market Access Strategy
• Clinical development strategy & Project Management
• Regulatory strategy
• Protocol/study optimization
• Study Feasibility

Clinical Operations
• Project Management
• Monitoring Services
• Regulatory
• Patient recruitment
• Data Management & Statistics
• Medical Writing
• Warehousing and Distribution
• Pharmacovigilance
• Lab services

Quality
• Conducting sponsor and investigational site audits
• Vendor assessments
• Developing or optimizing Quality Management Systems

Sponsors & Partners 2018
Main partner
Host sponsor
Host sponsor
Host sponsor
Platinum sponsor
Platinum sponsor
Platinum sponsor
Platinum sponsor
Gold sponsor
Silver sponsor
Award sponsor
Award sponsor
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