W H E N | When to engage us?
Regulatory strategy, problem solving, and pathway creation is what we do
GloboScience is the strategic regulatory problem solver and product development consulting partner of choice
Collaborating with clients at the forefront of advancing medical product development drives us. We focus exclusively on clients receiving devastating health authority responses or those needing to create a new regulatory pathway where none exists.
We do not augment staff or provide ancillary regulatory affairs services. Regulatory strategy, problem solving, and regulatory pathway creation is what we do.
Our expertise in transforming data from nonclinical and clinical development while levering these data to forging new regulatory pathways for medical products from concept to commercialization is unparalleled and our major differentiator.
We choose the clients we work with and the programs we work on. We solve problems, create a path forward, accelerate development, and then exit.
Health Authority Meetings
Therapeutic Programs
Countries
Our Expertise
From the laboratory to the approved product label, our expertise and influence extends globally.
Why Choose Us
Our experience working with products that comprise the 10 fastest FDA approvals, is our point of difference! Here are just a few reasons to choose GloboScience:
We Solve Problems
At GloboScience, we solve problems, we help you overcome challenges, we create regulatory strategies and pathways that results in first cycle approvals.
We Help You Avoid Pitfalls
We translate our client’s discoveries from the research bench and shepherds it through the myriad of challenges while avoiding pitfalls until it reaches the patient at the bedside.
We Are Transformative
Transforming our client’s nonclinical and clinical results into optimized or new regulatory pathways is what we do best. This translates into faster reviews, first cycle approvals, and products reaching the hands of prescribers and patients sooner.
You Gain Critical Insights
GloboScience has delivered sage and critical insights into regulators thinking for our clients at every step of the product development cycle across therapeutic areas, routes of administration and product types. We have successfully optimized hundreds of development programs for the medical products industry.
Unmatched Strategic Expertise
Our team of strategic regulatory experts bring a level of global experience and insights that are immeasurable (across geographic regions, development types, pathways and routes of administration). We are proud to have worked on the 10 Fastest FDA approved drugs during their life cycle.
We Deliver Wins for Clients
From rescuing programs with devastating clinical trial results or unfavorable health authority minutes, to optimizing clinical development programs and achieving shorter review and development time, we save our clients time and money, which translates into years of patient quality of life.
We Offer Breakthrough Regulatory Strategies
Our expertise in transforming data from nonclinical and clinical development while levering these data to forging new regulatory pathways for medical products from concept to commercialization is unparalleled and our major differentiator.
Accomplishments Drive Us
Collaborating with clients at the forefront of clinical science drives us. Our expertise in transforming and leveraging available date to forge new regulatory pathways for medical products from concept to commercialization is unparalleled and our major differentiator.
We Offer a Unique Perspective
Our unique perspective as a mix of prescribers, former sponsors and former reviewers from all regions of the world, coupled with our international success in guiding development programs makes us distinctly positioned to accelerate your path to approval.
We Help Fuel Your Growth
We’ve helped startups launch their first approved products. We’ve helped globally recognized brands along their product lifecycle and advanced our clinical-to-commercial client’s pipelines and fuel their growth.
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