Pharmaceutical Digital Transformationfor Medical Affairs Teams
We engineer GxP-compliant digital platforms, omnichannel Medical Affairs strategies, and HCP engagement portals built for scientific authority and clinical impact.
GDPR
Compliant
HIPAA
Compliant
SOC 2 Type II
In progress
ISO 27001
In progress
FDA 21 CFR Part 11
Compliant
WCAG 2.1 AA
Compliant
SSL / TLS 1.3
Compliant
OWASP Top 10
Aligned
GDPR
Compliant
HIPAA
Compliant
SOC 2 Type II
In progress
ISO 27001
In progress
FDA 21 CFR Part 11
Compliant
WCAG 2.1 AA
Compliant
SSL / TLS 1.3
Compliant
OWASP Top 10
Aligned
GDPR
Compliant
HIPAA
Compliant
SOC 2 Type II
In progress
ISO 27001
In progress
FDA 21 CFR Part 11
Compliant
WCAG 2.1 AA
Compliant
SSL / TLS 1.3
Compliant
OWASP Top 10
Aligned
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HCP Medical Portals
Secure gated platforms delivering essential clinical data to healthcare professionals.
MSL Field Presentations
GxP iPad decks integrated with Veeva Vault.
Omnichannel Strategy
Unified architecture for scientific content.
Clinical Trial Data Viz
Interactive dashboards for clinical trial data.
Virtual Advisory Boards
Secure environments for virtual KOL boards.
Interactive Congress Posters
Interactive digital formats for clinical abstracts at international congresses.
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The Industry Challenge
MLR review bottlenecks delay rollouts
Clinical trial data trapped in static PDFs
Disconnected omnichannel tools for MSLs & HCPs
Low adoption on rigid medical portals
GxP compliance & Veeva integration hurdles
The Numerikraft Approach
Compliance-by-design MLR approvals
Dynamic clinical trial data visualizations for KOLs
Omnichannel & MSL enablement
Intuitive HCP portals built for scientific clarity
Native GxP compliance & Veeva Vault integration
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We structure our design systems, content matrices, and handover documentation to streamline medical, legal, and regulatory (MLR) reviews, accelerating approval timelines for Advisory Board materials, congress posters, and collateral.
Every platform is architected with enterprise-grade security and strict data governance to protect sensitive patient and HCP information by design.
Our medical writers and scientific designers collaborate to ensure your clinical narrative remains accurate and impactful, from MoA animations to publication-ready congress posters.
Healthcare must be accessible to all. We design inclusive interfaces that meet strict accessibility standards for patients and professionals with diverse needs.
We develop scalable front-end architectures that integrate natively with Veeva and Salesforce Health Cloud, including CLM content for MSL iPads and approved email templates.
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We structure our design systems, content matrices, and handover documentation to streamline medical, legal, and regulatory (MLR) reviews, accelerating approval timelines for Advisory Board materials, congress posters, and collateral.
Every platform is architected with enterprise-grade security and strict data governance to protect sensitive patient and HCP information by design.
Our medical writers and scientific designers collaborate to ensure your clinical narrative remains accurate and impactful, from MoA animations to publication-ready congress posters.
Healthcare must be accessible to all. We design inclusive interfaces that meet strict accessibility standards for patients and professionals with diverse needs.
We develop scalable front-end architectures that integrate natively with Veeva and Salesforce Health Cloud, including CLM content for MSL iPads and approved email templates.
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01
Rapid Medical Onboarding
No delays. We start immediately with a precise understanding of your regulatory constraints, advisory board objectives, MSL field requirements, and congress timelines.
02
Scientific Strategy & MLR Alignment
We define a tailored strategy aligned with your therapeutic area goals, from KOL engagement plans to omnichannel content matrices and publication support.
03
Compliant Prototypes in Days
From wireframes to GxP-ready platforms, we craft validated assets: MSL iPad apps, interactive e-posters, HCP portals, and advisory board toolkits.
The true measure of Medical Affairs digital transformation isn't in the technology stack, it's in how seamlessly clinical evidence reaches the right Healthcare Professional, at the right moment.
Sid Ahmed MILI
Founder & CEO, Numerikraft
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/01
0%
MLR & Veeva Vault compliance
/02
0+
HCP portals & Advisory Boards
/03
0+
3D MoA & Data Viz assets
/04
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Validated interactive prototyping
/05
0%
NDA & GxP data security
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Want to see
more work?
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NDA? Of course.
We're used to working in confidential, regulated environments.
Fast response.
We get back to you within 24h — sharp, structured, and relevant.
No juniors.
Work directly with senior experts in design, strategy, and digital delivery.
Regulated? No problem.
We speak your language — scientific, compliant, and scalable.
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We apply a 'compliance-by-design' engineering methodology. Before initiating UI design, we map promotional and non-promotional boundaries alongside Medical, Legal, and Regulatory (MLR) review criteria. This structural rigor eliminates friction during internal committee audits, accelerating approval cycles for global medical teams.
Absolutely. Our engineering and design teams build front-end architectures specifically structured for enterprise pharmaceutical ecosystems. We master Veeva Vault PromoMats export specifications, MSL iPad CLM (Closed-Loop Marketing) content integration, Veeva Approved Emails, and seamless interoperability with Salesforce Health Cloud and specialized headless CMS frameworks.
Yes. We create institutional and scientific brand identity systems engineered to reflect the clinical value of your molecules and trials. We deliver comprehensive Brand Books and Design Systems that ensure visual consistency and narrative authority across all digital touchpoints (HCP portals, congresses, MSL enablement).
Yes. Our scientific designers and art directors produce photorealistic 3D Mechanism of Action (MoA) animations and interactive models. We translate complex preclinical and clinical trial data into high-precision visual narratives designed to engage Key Opinion Leaders (KOLs), investigators, and healthcare professionals.
Yes. We engineer private, secure digital environments tailored for virtual and hybrid Advisory Board meetings. Our platforms streamline interactive clinical trial presentations, secure event logistics, and real-time capture of strategic insights from international Key Opinion Leaders.
We architect token-based Design Systems capable of dynamically switching between Latin alphabets (English, French) and Right-To-Left (RTL) formatting for Arabic. This i18n framework guarantees typography control, component alignment, and flawless multi-region rollouts across North Africa and the Middle East.
Yes, our agency maintains deep familiarity with medical communication frameworks governed by the ANSM in France and the Ministry of Health in Algeria. We ensure that the localization and deployment of your global digital assets strictly adhere to local promotional laws and regulatory guidelines.
Data security and intellectual property protection are absolute priorities. We systematically operate under strict non-disclosure agreements (NDAs). Our engineering infrastructure and workflows follow GxP guidelines, HIPAA requirements for protected health information (PHI), and GDPR standards, safeguarding your patents and clinical assets at every stage.