Regulatory Health Economic Expert Resources - VCLS

Time 2020-12-07 21:04:49

Web Name: Regulatory Health Economic Expert Resources - VCLS

WebSite: http://voisinconsulting.com

ID:126844

Keywords:

Economic,Health,Regulatory,

Description:

Delivering innovative medical solutions to patients together VCLS supports life science companies and engages in communication with regulators and payers. We partner with Biotech, Pharma and Medtech manufacturers to develop, register and launch innovative products globally. Learn more People-powered solutions The regulatory landscape is constantly evolving. At VCLS, we thrive on innovation.Finding new ways of achieving our clients’ goals keeps us at the forefront of an ever-changing environment. De-risk your digital health technology development by applying appropriate regulatory framework at early stage. Learn more Gene therapy, somatic or stem cell therapy and tissue engineering are at the cutting edge of translational research. Learn more Microbiome health products – drugs or foods? Here are some key considerations such as health claim you wish to make, the target population, budget and development timelines in developing such products. Learn more Our solutions for each stage of development Regulatory challenges vary at each stage of product development – when to interact with health authorities? Is a pediatric development plan necessary? Are clinical trial results adequate for both regulatory approval and market access? We recognize the importance of strategic analysis and decision-making in drug and medical device development. Our tailored solutions are adapted to your product development stage and we proactively tackle the challenges being faced. presentation FDA Deep Dive into FDA’s Expedited Programs for Drug Development If you are developing products for serious and life-threatening illnesses with unmet medical needs, there are several mechanisms offered by blog Digital health New Guidance on Clinical Evaluation of Medical Device Software The Medical Device Coordination Group (MDCG) recently published a new guidance entitled “Guidance on Clinical Evaluation (MDR) / Performance Evaluation webinar EMA Unlocking the EMA Meetings: the Process and How to Prepare Adequately Clear strategy, compelling argument and well-rehearsed preparation are all key to having a successful EMA meeting, no matter if it publication A Regulatory Landscape Shift for In Silico Clinical Trials Modelling and simulation (M S) has grown to become a reliable approach to better understand and optimize key decisions related to Career at VCLS VCLS helps biotech, pharma and med tech companies delivering innovative therapies to patients. We are passionate about what we do, we dare to be different and challenge the status quo, while focusing on our mission of being the global partner to expedite access of HealthTech products to regulated markets. See open positions*I have read and agreed to the Terms of Use and the Privacy Policy.Yes, I would like to receive communications regarding VCLS services and events Send " data-content="Rue des Îles Kerguelen, Parc Edonia, Bâtiment M, 35760 Saint-Grégoire, FrancePhone : +33 (0) 2 99 68 71 10Fax : +33 (0)1 41 31 83 09See on Google Map" d="M376.9,137.8c0,0.6-0.1,1-0.3,1.4l-2.8,6c-0.1,0.2-0.2,0.3-0.4,0.4c-0.2,0.1-0.3,0.1-0.5,0.1s-0.4,0-0.5-0.1 c-0.2-0.1-0.3-0.2-0.4-0.4l-2.9-6c-0.2-0.4-0.3-0.8-0.3-1.4c0-1.1,0.4-2,1.2-2.8c0.8-0.8,1.7-1.2,2.8-1.2c1.1,0,2,0.4,2.8,1.2 C376.5,135.7,376.9,136.7,376.9,137.8z M374.3,139.2c0.4-0.4,0.6-0.9,0.6-1.4c0-0.6-0.2-1-0.6-1.4c-0.4-0.4-0.9-0.6-1.4-0.6 c-0.6,0-1,0.2-1.4,0.6c-0.4,0.4-0.6,0.9-0.6,1.4c0,0.6,0.2,1,0.6,1.4c0.4,0.4,0.9,0.6,1.4,0.6C373.4,139.8,373.9,139.6,374.3,139.2 z"/> " data-content="Innovation House, Albany Park, Camberley, Surrey GU16 7PL, UKPhone : +44 (0) 1276 671 166Fax : +44 (0) 1276 670 960See on Google Map" 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TAGS:Economic Health Regulatory 

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Global Product Development Strategy – Communication with Regulators & Payers. Discover how VCLS helps pharmaceutical, biotechnology and medical device companies on designing and implement innovative, efficient regulatory strategies, clinical trials, drug safety and vigilance management from pre-approval to post-approval activitiescommercialization.

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