Expert Insights
Become a Contributer!
We are seeking industry experts who are eager to share fresh perspectives on FDA regulatory pathways, compliance strategies, and industry trends.
Expert Insights: Regulatory & Beyond aims to be the premier platform for sharing cutting-edge perspectives on regulatory and compliance topics. By featuring voices from across the spectrum—from regulatory professionals to industry veterans and emerging experts—we provide actionable knowledge and diverse viewpoints on today’s regulatory challenges.
If you’re an expert in regulatory or compliance fields and would like to contribute your perspective, we’d love to hear from you! Submit a proposal below and join a growing network of professionals shaping industry discussions.
What We’re Looking For:
- Original, insightful content focused on FDA regulations, compliance best practices, industry trends, regulatory challenges, case studies, and the potential regulatory impact of emerging technologies.
- Practical advice, how-to’s, and actionable strategies for companies navigating the FDA regulatory landscape.
- Insights into how the US FDA regulatory landscape for a particular industry or product type compares to the global regulatory landscape at large.
- Analysis of current FDA guidelines, regulatory updates, or specific industry challenges for the FDA-regulated industries we serve.
- Articles that align with our mission to support small to mid-sized companies in bringing innovative products to market and maintaining compliance throughout the product lifecycle, especially start-up companies.
Submit Your Proposal Today to [email protected]
and Become A Contributor
Proposal Submission Guidelines
Send your guest contributor proposal to [email protected] with the subject line: “Expert Insights Proposal: [Article Topic]”.
Your submission should include the following:
- Proposed Title & Topic Summary:
- A working title for your proposed article.
- A brief overview (150-200 words) summarizing the key points and value your article will provide to our audience.
- Outline:
- A detailed outline of the content you plan to cover (bullet points are fine).
- Target Audience:
- Specify the intended audience for your article (e.g., medical device startups, foreign manufacturers, other regulatory professionals, investors).
- Author Bio:
- A brief bio (50-100 words) highlighting your expertise and relevant experience. Include a professional headshot and links to your LinkedIn profile and any relevant publications.
- Writing Sample (optional):
- If available, please include a sample of your previous work.
Current Topics Of Interest
While we are open to receiving proposals on all current and relevant topics to the FDA regulated product space, we are particularly interested in content that explores the following key topics:
Cybersecurity in healthcare and medical devices
How Changes in US Administration Could Impact Regulated Industries
New FDA guidances and their implications for industry stakeholders
Case Studies on New and Innovative Technologies
Ai and it’s impact on the Medtech industry
Lessons the US regulatory landscape could learn from foreign regulatory bodies
Submit Your Proposal Today!
Next proposal deadline: February 3, 2025.
We will be selecting one to two articles monthly for publication. Accepted writers will be notified within 7 days of the proposal deadline, with final articles due within approximately three weeks of notification. Our team will provide minor editing support and a final review of the article prior to publishing. Articles will typically be published within the first two weeks of the month following article submission (for example, proposals selected in December will be published in January). Writers will receive an email notifying them of publication once the article is live on our website and on our LinkedIn page.
View the full proposal schedule and terms and conditions below before submitting your proposal.
