AI consulting for the pharma industry

Innowise helps pharmaceutical companies harness AI to shorten discovery timelines, optimize clinical operations, ensure GxP compliance, and create scalable solutions ready for global markets.

15+

farma AI adviseurs

50+

ingenieurs gespecialiseerd in farma

40+

AI-gedreven farmaceutische projecten opgeleverd

Innowise helps pharmaceutical companies harness AI to shorten discovery timelines, optimize clinical operations, ensure GxP compliance, and create scalable solutions ready for global markets.

15+

farma AI adviseurs

50+

ingenieurs gespecialiseerd in farma

40+

AI-gedreven farmaceutische projecten opgeleverd

Our AI development services for pharmaceuticals

We support pharmaceutical companies across the entire drug development lifecycle with consulting and hands-on development.

Advies

Use case validation

PoC/MVP development

AI implementation and integration

Custom AI solution development

AI voor naleving van regelgeving

Advies

Guiding pharma leaders through AI adoption with strategic assessments and roadmap design. We clarify priorities, highlight high‑value opportunities across R&D and clinical trials, and ensure alignment with scientific and business goals.

Use case validation

Evaluating hypotheses with data analysis and pilot models to confirm feasibility. We help you avoid sunk costs by testing assumptions early and validating data readiness before scaling.

PoC/MVP development

Designing and delivering focused prototypes that demonstrate tangible value. In 8-12 weeks, our teams implement small‑scale AI models with clear KPIs and detailed test plans, giving your stakeholders evidence for confident go/no‑go decisions.

AI implementation and integration

Engineering and embedding validated AI models into your IT ecosystem — from CTMS and LIMS to ERP platforms. In doing so, we ensure robust security, interoperability, and scalability so adoption is seamless for your research and operations teams.

Custom AI solution development

Developing end‑to‑end AI pipelines tailored to specific pharmaceutical workflows. This includes multi‑omics analytics for target discovery, predictive modeling for trial outcomes, advanced pharmacovigilance NLP, and more. Each solution is engineered for reliability, interpretability, and regulatory alignment.

AI voor naleving van regelgeving

Building AI‑powered systems that simplify complex compliance tasks. Examples include automating audit preparation, continuously monitoring regulatory updates, validating datasets at scale, and streamlining reporting flows — all reducing manual burden while meeting FDA, EMA, and GxP standards.

Advies

Use case validation

Evaluating hypotheses with data analysis and pilot models to confirm feasibility. We help you avoid sunk costs by testing assumptions early and validating data readiness before scaling.

PoC/MVP development

AI implementation and integration

Custom AI solution development

AI voor naleving van regelgeving

Areas we help improve with AI

Our AI consulting and development services target critical pharma challenges across research, operations, and compliance.

Drug design & discovery

Accelerate target identification and hit-to-lead selection with multi‑omics, generative models, and advanced simulation methods.

Pharma R&D

Enhance early discovery and translational research with analytics pipelines that reveal hidden correlations and provide actionable insights.

Clinical trials optimization

Improve recruitment and adaptive design with predictive analytics and enable real-time monitoring to spot risks or opportunities sooner.

Ensure adherence to GLP, GCP, GMP, GDP, and GVP standards with validated, compliant AI systems.

Clinical intelligence

Unlock insights from EHR, imaging, and trial datasets to guide evidence-based decision-making.

Manufacturing & supply chain

Predict demand, optimize batch quality, and prevent bottlenecks with AI-driven process monitoring.

Pharmacovigilance

Detect safety signals across clinical reports, publications, and social media using NLP and ML.

Compliance & risk management

Embed auditability, explainability, and data security into every AI workflow.

Vendor procurement

Streamline supplier selection and monitoring with intelligent data analysis.

AI solutions we build for pharma

We design and implement specialized AI applications that address the unique needs of pharmaceutical R&D and operations, from trial automation to personalized medicine, ensuring each solution is practical, compliant, and ready to scale.

Pharmacovigilance & drug safety systems

Monitor adverse events in real time across multiple data streams, using NLP to flag weak signals early and automate safety reporting.

Automated clinical trial management

Digitize CTMS and EDC workflows to streamline recruitment and adaptive monitoring, enabling faster protocol adjustments and stronger data integrity.

Real-time data capturing platforms

Integrate EHR, lab, and device data into unified datasets that are ready for downstream analytics and regulatory submissions.

Regulatory compliance automation

Automate audit preparation and CAPA tracking with built-in validation frameworks that simplify inspections and reduce risk.

AI-based pharma supply chain management

Forecast demand and optimize inventory levels while proactively identifying shortages with predictive models linked to production data.

Predictive analytics for market trends

Spot emerging therapeutic opportunities and track competitor pipelines to inform portfolio strategy and market entry decisions.

Drug repurposing platforms

Mine real-world evidence and omics datasets to identify new indications for existing molecules, lowering development costs and time-to-market.

Personalized medicine platforms

Enable biomarker discovery and therapy matching by combining omics data with clinical records for targeted treatment strategies.

Omics data integration platforms

Connect genomics, proteomics, and metabolomics datasets into a cohesive view, supporting biomarker discovery and disease pathway analysis.

In pharma, AI succeeds when it delivers insights researchers can trust and act on quickly. It’s not about building massive systems upfront but about proving value in one workflow, then scaling responsibly so adoption feels natural and compliance is never in doubt.

Anastasia Ilkevich

Portfolio manager in Healthcare and Pharmaceutical technologies

Agentic AI as the new frontier in pharma

We also develop AI agents as standalone solutions to streamline pharmaceutical processes. These are autonomous, goal-driven systems that can plan, reason, and act with minimal human intervention, unlocking entirely new possibilities:

01/04

Versnelde ontdekking van geneesmiddelen

AI agents explore vast molecular libraries, propose novel compounds with generative models, and refine promising leads, compressing discovery timelines that traditionally take years into months.

02/04

Smarter clinical trials

Agentic systems design adaptive trial protocols, match patients to studies more effectively, and adjust in real time as new data streams in, helping sponsors reduce recruitment delays and trial failures.

03/04

Intelligent workflows

By automating literature reviews, orchestrating lab tasks, and prioritizing experimental pipelines, agentic AI removes manual bottlenecks and allows researchers to dedicate more time to scientific exploration.

04/04

Continuous compliance

AI agents track regulatory changes across FDA, EMA, and ICH guidelines, automate documentation, and proactively flag risks so companies stay inspection‑ready at all times.

Versnelde ontdekking van geneesmiddelen

Smarter clinical trials

Intelligent workflows

Continuous compliance

Our approach to AI consulting for pharma

Our consulting approach is built to deliver measurable results for pharma organizations by combining technical expertise with a deep awareness of industry regulations and scientific realities.

Strategic roadmap & scoping

We’ll team up with you to define project scope, goals, and regulatory considerations. This includes aligning on scientific objectives, understanding the data landscape (from omics to clinical trial data), and establishing milestones that keep drug development programs on track.

Feasibility analysis & cost optimization

We’ll conduct a thorough feasibility check with a focus on scientific rigor, regulatory approval, and ROI. By identifying risks early, optimizing resource allocation, and planning around compliance costs, we maximize both financial and scientific returns.

Samenwerkingsverband

Projects thrive when pharma teams and technology experts work as one. We build open communication into every engagement so that your stakeholders stay aligned, decisions remain transparent, and outcomes are robust enough to withstand scientific and regulatory scrutiny.

Kwaliteit assurance

We maintain the highest quality standards through rigorous testing, model validation, bias checks, and traceability protocols required by GxP. Both automated QA and expert engineering review guarantee robustness and reproducibility.

Gegevensbeveiliging en compliance

Your sensitive patient, trial, and research data will be treated with the strictest security standards. Audit‑ready pipelines; HIPAA, GDPR, FDA, and EMA compliance; and ISO 27001 practices — all ensure safe AI adoption without compromising data integrity.

Knowledge transfer & documentation

As a result of our cooperation, your teams will be fully equipped through detailed documentation, validation reports, and training. This makes regulatory reviews smoother and sustains long‑term value from AI initiatives.

Strategic partnerships in pharma AI

We collaborate with leading pharma companies, research institutions, and technology providers to co-develop AI solutions that are both innovative and compliant.

Start your AI journey

Secure a clear, compliance-ready roadmap that validates a high-impact use case and generates measurable outcomes for your stakeholders and teams.

Geselecteerde succesverhalen

Explore real-world examples of how we’ve helped pharmaceutical clients cut costs, improve trial efficiency, and discover new therapies.

Waarom kiezen voor Innowise

Partnering with Innowise means relying on a team that blends technical excellence with deep pharmaceutical expertise. We help clients avoid costly missteps, accelerate time-to-value, and ensure compliance from day one.

Deep pharma expertise

Work with 50+ specialists experienced in R&D, clinical trials, regulatory submissions, and compliance audits.

Regulatory-first design

Stay aligned with HIPAA, GDPR, FDA, EMA, and GxP standards thanks to validated pipelines, audit-ready documentation, and secure data handling.

Proven delivery model

Leverage our experience from 40+ pharma AI projects where we delivered measurable business outcomes and scientific insights.

Ondersteuning van begin tot eind

From early advisory to custom solution engineering and long-term MLOps, we support every stage of AI adoption.

Flexibele betrokkenheid

Choose from staff augmentation, co-development, or fully outsourced delivery models to match your budget and resource needs.

Wat onze klanten vinden

Explore verified reviews and customer success stories from organizations we support.

Marco Scarpa Technisch productbeheerder Beantech S.r.l

"Het was een zeer intensieve en effectieve samenwerking, alle ontwikkelaars waren gefocust op de doelen en voorbereid op alle technologieën die we behandelen."

Industrie IT-diensten
Grootte van het team 6 specialisten
Duur 22+ maanden
Diensten IoT-ontwikkeling

Nikolaj Orlov CEO KEYtec AG

"Wat ik het meest indrukwekkend vond aan Innowise was hun vermogen om zich aan te passen aan onze specifieke behoeften met behoud van strikte tijdlijnen. Ze combineerden een klantgerichte aanpak met sterke projectmanagementvaardigheden, waardoor de deliverables van hoge kwaliteit en op tijd waren."

Industrie Financiële diensten
Grootte van het team 2 specialisten
Duur 8 maanden
Diensten IT-beheerde diensten

Gian Luca De Bonis CEO & CTO Enable Development OÜ

"We zijn onder de indruk van hun flexibiliteit en bereidheid om oplossingen te vinden voor uitdagende situaties. Ze hebben actief geholpen in alle soorten situaties. De bereidheid van het team om optimale resultaten te leveren verzekert het succes van de samenwerking."

Industrie IT-advies
Grootte van het team 8 specialisten
Duur 36 maanden
Diensten Personeelsuitbreiding

FAQ about AI in the pharma industry

AI helps accelerate drug discovery, optimize clinical trials, improve manufacturing efficiency, and strengthen compliance processes. Use cases range from virtual compound screening and biomarker discovery to trial recruitment optimization and pharmacovigilance.

By combining multi-omics data with in silico screening, molecular docking, and generative design, AI reduces discovery cycles from years to months while increasing the likelihood of identifying viable leads.

Yes. We design systems that meet FDA, EMA, HIPAA, GDPR, and GxP requirements through data minimization, explainable models, validation frameworks, and detailed audit trails.

Analysts project the global pharma AI market to grow into the tens of billions of dollars within the next decade, driven by adoption in discovery, trials, pharmacovigilance, and manufacturing.

Maak gerust een afspraak om alle antwoorden te krijgen die je nodig hebt.

Boek een gesprek

Contacteer ons

Boek een gesprek of vul het onderstaande formulier in en we nemen contact met je op zodra we je aanvraag hebben verwerkt.

Naam

Bedrijf

E-mail

Telefoon

Bericht

Stuur ons een spraakbericht

Documenten bijvoegen

Bestand uploaden

Je kunt 1 bestand van maximaal 2 MB bijvoegen. Geldige bestandsformaten: pdf, jpg, jpeg, png.

Door op Verzenden te klikken, stemt u ermee in dat Innowise uw persoonsgegevens verwerkt volgens onze Privacybeleid om u van relevante informatie te voorzien. Door je telefoonnummer op te geven, ga je ermee akkoord dat we contact met je opnemen via telefoongesprekken, sms en messaging-apps. Bellen, berichten en datatarieven kunnen van toepassing zijn.

U kunt ons ook uw verzoek sturen
naar contact@innowise.com

Wat gebeurt er nu?

Zodra we je aanvraag hebben ontvangen en verwerkt, nemen we contact met je op om de details van je projectbehoeften en tekenen we een NDA om vertrouwelijkheid te garanderen.

Na het bestuderen van uw wensen, behoeften en verwachtingen zal ons team een projectvoorstel opstellen met de omvang van het werk, de teamgrootte, de tijd en de geschatte kosten voorstel met de omvang van het werk, de grootte van het team, de tijd en de geschatte kosten.

We zullen een afspraak met je maken om het aanbod te bespreken en de details vast te leggen.

Tot slot tekenen we een contract en gaan we meteen aan de slag met je project.

AI consulting for the pharma industry

Our AI development services for pharmaceuticals

Advies

Use case validation

PoC/MVP development

AI implementation and integration

Custom AI solution development

AI voor naleving van regelgeving

Areas we help improve with AI

Drug design & discovery

Pharma R&D

Clinical trials optimization

GxP

Clinical intelligence

Manufacturing & supply chain

Pharmacovigilance

Compliance & risk management

Vendor procurement

AI solutions we build for pharma

Pharmacovigilance & drug safety systems

Automated clinical trial management

Real-time data capturing platforms

Regulatory compliance automation

AI-based pharma supply chain management

Predictive analytics for market trends

Drug repurposing platforms

Personalized medicine platforms

Omics data integration platforms

Agentic AI as the new frontier in pharma

Our approach to AI consulting for pharma

Strategic partnerships in pharma AI

Geselecteerde succesverhalen

Waarom kiezen voor Innowise

Deep pharma expertise

Regulatory-first design

Proven delivery model

Ondersteuning van begin tot eind

Flexibele betrokkenheid

Wat onze klanten vinden

FAQ about AI in the pharma industry

Contacteer ons

Wat gebeurt er nu?

Heb je andere diensten nodig?

Inhoudsopgave