Medical Affairs & Evidence
split-image
first

Medical Affairs & Evidence

Medical affairs and evidence generation teams are converging as a strategic powerhouse. ZS helps you lead the way by scaling science, insights and customer engagement at every stage in the product life cycle.

Your teams are doing more than supplying information in a compliant way—you’re shaping medical affairs strategy while generating and communicating the right evidence that improves patient lives from research to bedside. ZS helps teams focus their medical affairs and evidence strategy, strengthen execution and scale impact by lending expert support and implementing ready-to-use products and compliant platforms built for your day-to-day needs. We help you do more of what matters—faster and with confidence.
true
white
Research & Development
true
Let’s connect
/content/zs/en/forms/lets-connect-capabilities
primary
Second Button CTA Text
#
secondary
default

Challenges we solve

center
white
Eyebrow Text
Button CTA Text
#
primary
default
Design your medical affairs strategy

Be ready for what’s ahead. ZS can help you define your team’s purpose, prepare for future changes, offer necessary training and implement measurement levers.

Scale with purpose

Introduce scalable medical affairs tech, planning and insights that suit your company’s unique needs. Every organization is different, so there’s no need to follow a template. From organizational design to field team deployment and innovative tech solutions, ZS can help.

Design your scientific evidence generation plan

ZS helps R&D organizations with integrated evidence strategy, planning and generation. Our solutions like ZS Evidence Pro empower you to adopt the multidisciplinary approach that medical evidence generation requires, while ZS experts focus on global health economics outcomes research (HEOR), clinical operations and real-world evidence (RWE) to help provide patients with access to innovative medical interventions.

Articulate medical affairs’ value

Identify, understand and articulate the value that medical affairs creates for both internal and external stakeholders. ZS can help you demonstrate your unique benefit to the organization.

default

Our client impact

center
white
Eyebrow Text
Button CTA Text
#
primary
default
100+
Clients globally
Learn more about hours spent on learning and development in 2024
3,000+
Key opinion leaders (KOLs) engaged in assessing medical science liaison (MSL) role effectiveness
Learn More
Learn more about hours spent on learning and development in 2024
75+
Disease areas of expertise
Learn More
Learn more about hours spent on learning and development in 2024
default
left
white
Eyebrow Text
Button CTA Text
#
primary
default
default

Our approach

left
false
grey
Subhead / Eyebrow Text
Button CTA Text
#
primary
default
light-accordion-a
single
Lead the charge in elevating health outcomes
h3
ZS helps you shape medical affairs strategy, close care gaps and generate critical knowledge to build truly patient-centered healthcare solutions throughout the life sciences product life cycle.
false
Call to action
#
Work hand-in-hand with experts across silos and therapy areas
h3
ZS’s multidisciplinary team of seasoned experts connect science, regulatory and patient-focused strategies at your organization.
false
Call to action
#
Innovate at scale throughout the product life cycle
h3
ZS helps medical affairs innovation teams like yours scale success, drive value and prove impact.
false
Call to action
#
Elevate your impact with an intelligent medical affairs platform
h3
ZS helps you create a truly connected ecosystem. ZAIDYN®, our intelligent, cloud-native software platform powers collaboration to deliver compliant, impactful scientific engagement with healthcare professionals.
false
Call to action
#
default

Explore our products and capabilities

left
false
grey
Eyebrow Text
Button CTA Text
#
primary
default
image
ZAIDYN®
h3
ZAIDYN®
Unify data, analytics and workflows across commercial, medical and patient teams on one AI-powered life sciences intelligence platform.
Let's go
/content/zs/en/products/zaidyn-platform
ZS evidence pro
h3
ZS Evidence Pro
Reimagine the integrated evidence workflow. ZS Evidence Pro features intuitive dashboards for planning across therapeutic areas and organizations.
Request a demo
/content/zs/en/forms/contact-us
ZAIDYN® medical
h3
ZAIDYN® Medical
Transform scientific engagement and evidence generation with AI-driven insight discovery, opinion leader intelligence and real-world data analytics, helping medical teams accelerate evidence creation and amplify scientific impact.
Let's go
/content/zs/en/products/zaidyn-platform/medical
RBQM360
h3
risk based monitoring
RBQM 360 is ZS’s centralized risk-based monitoring solution that helps sponsors detect issues early, reduce trial risk and improve data quality across global study portfolios.
Learn more
/content/zs/en/forms/contact-us
ZAIDYN® clinical development
h3
clinical development
ZS’s purpose-built platform helps clinical teams design smarter trials, connect data and automate workflows to speed execution and improve decision-making.
Learn more
/content/zs/en/forms/contact-us
default

Frequently asked questions about our medical affairs and evidence solutions

left
false
grey
Subhead / Eyebrow Text
Button CTA Text
#
primary
default
light-accordion-a
single
How can ZS help my medical affairs team scale its impact?
h3
Take the guesswork out of determining the right size, structure and geographic alignment of your medical affairs organization. ZS works with field medical affairs managers to optimize the size of MSL teams and design territory maps based on business criteria and workload metrics. We have also outlined a roadmap to advance your organization’s progress toward measurable, scalable and sustainable medical affairs impact.
false
Call to action
#
What products and platforms does ZS offer for medical evidence generation?
h3
ZS’s AI, machine learning and data-driven technologies can help track medical evidence generation, identify and optimize trial sites for phase 4 clinical studies, and generally free up medical affairs leaders to focus on personal engagement and evidence dissemination. Through ZAIDYN® solutions, ZS Evidence Pro and our other technology offerings, ZS helps you tackle common medical affairs challenges.
false
Call to action
#
How does ZS support integrated evidence planning across functions?
h3
With solutions like ZS Evidence Pro, our integrated evidence planning (IEP) approach empowers you to establish robust plans that meet your evidence needs. If you want to accelerate approval, enhance market access, differentiate your product’s value and deliver relevant insights for key decision-makers, ZS can help. We start by reducing silos, which empowers leaders to implement IEPs and cross-team data strategy—part of our overall strategy of helping organizations master complex ecosystems of data. We also help define standard lexicons, templates, frameworks, guidelines, playbooks and digital tools to power integrated evidence across the organization. And we constantly assess the market landscape to enhance your future IEPs.
false
Call to action
#
How does ZS approach compliance in medical affairs and evidence services?
h3
Regulatory risk in your market carries a high cost, so ZS takes a compliance-first strategy. Our compliance experts partner with yours every step of the way so your ideas can come to life and bring real impact. From concept to implementation, we help you innovate, launch, scale and evolve your ideas with confidence. As a business strategy consulting firm with expertise in both medical science and marketing, ZS can tailor our work to the fine line you walk.
false
Call to action
#
What guardrails do you have between commercial and medical?
h3
Our experts innovate with compliance guardrails in place every step of the way so your good ideas can come to life and bring real impact. We thread the compliance practice throughout the process, so you won't hit a wall at the end of the project. Our medical and pharmaceutical compliance experts have a seat at the table from the first discussions in a strategy project, as well as in the development of our solutions and platforms. This ensures we don’t waste time developing a solution that crosses a regulatory line.
false
Call to action
#
default

Meet our experts

left
false
grey
Eyebrow Text
Button CTA Text
#
primary
default