This white paper is a companion piece to our popular webinar where we share some of the best approaches we have discovered for Corporate Scientific Communication Strategies.
A well-developed and well-executed Scientific Communication Plan can have positive impact on market awareness and company goals. This requires top-level, strategic perspective, and project level review and discussion to effectively frame the message. Multi-disciplinary planning, goal-oriented strategies, and project level-checks are just some of the important aspects of data-driven clinical and scientific communications that maximize market impact. But, who among your team are the right people to be assigned the task of preparing, supporting, and pushing along a written project to completion?
The best advice we can give is taken from …
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Get a copy of the slides from this webinar or click to watch the recording.
A comprehensive scientific communications program is a critical tool for medical device, in vitro diagnostic and pharma companies to raise market awareness for their products. Done well, effective “real-world” communication can position your company as a key scientific leader in its field and drive market adoption and sales. However, ineffective or poorly executed scientific communications can result in lost opportunities to make an early, meaningful and even a positive impact on the market.
In this practical presentation, President Laurie Mitchell: 1) discusses how an effective scientific communication plan is an important marketing tool for an organization, and 2) presents five strategies to ensure your corporate objectives are supported and maximize the real-world impact of your data. Watch to learn how this applies to your organization and how to implement these strategies into your current processes.
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Criterion Edge has the expertise and resources to do literature reviews for many types of documents. Ready for a free consult?
Fill out this form, or contact us at info@criterionedge.com, and we would be happy to answer any of your questions as well as book you an appointment to discuss your project needs during a time that works for you.
In this discussion, we provide an overview of how to plan and coordinate change within an organization to meet upcoming EU IVDR regulatory requirements. We will be highlighting key steps involved in helping medical affairs transition to a more rigorous regulatory environments, and how to evaluate talent gaps, team leadership composition, and process challenges of your product portfolio.
In this discussion, our panel of proven leaders discuss the key elements that support and propel the innovation process in the medical device, pharmaceutical, and IVD industries. We will be highlighting key areas of the process, important players in the pathway to the market, and how successful innovations spawn new innovations in new markets such as the digital health space, and more.
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