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+

pharma AI konsulter

50+

ingenjörer som specialiserar sig på läkemedel

40+

AI-drivna läkemedelsprojekt levererade

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+

pharma AI konsulter

50+

ingenjörer som specialiserar sig på läkemedel

40+

AI-drivna läkemedelsprojekt levererade

  • Rådgivning
  • Use case validation
  • PoC/MVP development
  • AI implementation and integration
  • Custom AI solution development
  • AI för efterlevnad av regelverk

Rådgivning

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.

Rådgivning

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.

Use case validation

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.

PoC/MVP development

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.

AI implementation and integration

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.

Custom AI solution development

AI för efterlevnad av regelverk

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.

AI för efterlevnad av regelverk
Rådgivning

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.

Rådgivning
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.

Use case validation
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.

PoC/MVP development
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.

AI implementation and integration
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.

Custom AI solution development
AI för efterlevnad av regelverk

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.

AI för efterlevnad av regelverk

Areas we help improve with AI

  • 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.

  • GxP

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

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.

Portfolio manager in Healthcare and Pharmaceutical technologies

Agentic AI as the new frontier in pharma

01/04

Snabbare upptäckt av läkemedel

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.

01

Snabbare upptäckt av läkemedel

02

Smarter clinical trials

03

Intelligent workflows

04

Continuous compliance

Our approach to AI consulting for pharma

Strategic roadmap & scoping Ikon

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 Ikon

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.

Samarbetspartnerskap Ikon

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.

Kvalitet försäkring Ikon

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.

Datasäkerhet och efterlevnad Ikon

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 Ikon

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

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Novartis logotyp.Alliance Medical-logotypen.ISO 27001-logotyp.HIPAA-logotyp.GDPR-logotyp.Teleas logotyp. Megaomega logotyp. NAIP:s logotyp.
Novartis logotyp. Alliance Medical-logotypen. ISO 27001-logotyp. HIPAA-logotyp.
Novartis logotyp. Alliance Medical-logotypen. ISO 27001-logotyp. HIPAA-logotyp.
GDPR-logotyp. Teleas logotyp. Megaomega logotyp. NAIP:s logotyp.
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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.

Utvalda framgångshistorier

Googles logotyp. Hays logotyp. PayPal-logotyp. Siemens logotyp. Nike-logotyp. Volkswagen-logotyp. LVMH:s logotyp. Nestle-logotyp. Novartis logotyp. Spotify-logotyp.
Googles logotyp. Hays logotyp. PayPal-logotyp. Siemens logotyp. Nike-logotyp. Volkswagen-logotyp. LVMH:s logotyp. Nestle-logotyp. Novartis logotyp. Spotify-logotyp.
Aramcos logotyp Mercedes logotyp. Costco Wholesale logotyp. Logotyp för skal. Accentures logotyp. NVIDIA-logotyp. SPAR-logotypen. Mastercard-logotyp. CVS Healths logotyp. Walt Disney-logotypen.
Aramcos logotyp Mercedes logotyp. Costco Wholesale logotyp. Logotyp för skal. Accentures logotyp. NVIDIA-logotyp. SPAR-logotypen. Mastercard-logotyp. CVS Healths logotyp. Walt Disney-logotypen.
Googles logotyp.Hays logotyp.PayPal-logotyp.Siemens logotyp.Nike-logotyp.Volkswagen-logotyp.LVMH:s logotyp.
Googles logotyp.Hays logotyp.PayPal-logotyp.Siemens logotyp.Nike-logotyp.Volkswagen-logotyp.LVMH:s logotyp.
Nestle-logotyp.Novartis logotyp.Spotify-logotyp.Aramcos logotyp.Mercedes logotyp.Costco Wholesale logotyp.
Nestle-logotyp.Novartis logotyp.Spotify-logotyp.Aramcos logotyp.Mercedes logotyp.Costco Wholesale logotyp.
Logotyp för skal.Accentures logotyp.NVIDIA-logotyp. SPAR-logotypen.Mastercard-logotyp.CVS Healths logotyp.Walt Disney-logotypen.
Logotyp för skal.Accentures logotyp.NVIDIA-logotyp. SPAR-logotypen.Mastercard-logotyp.CVS Healths logotyp.Walt Disney-logotypen.

Varför välja Innowise

  • 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.

  • Stöd från början till slut

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

  • Flexibelt engagemang

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

Vad våra kunder tycker

Marco Scarpa Teknisk produktchef Beantech S.r.l.
företagets logotyp

"Det var ett mycket intensivt och effektivt samarbete, alla utvecklare var fokuserade på målen och förberedda på alla de tekniker vi täcker."

  • Industri IT-tjänster
  • Teamstorlek 6 specialister
  • Varaktighet 22+ månader
  • Tjänster IoT-utveckling
Nikolaj Orlov VD KEYtec AG
företagets logotyp

"Det jag tyckte var mest imponerande med Innowise var deras förmåga att anpassa sig till våra specifika behov och samtidigt hålla strikta tidsramar. De kombinerade ett kundcentrerat förhållningssätt med starka projektledaregenskaper och såg till att leveranserna höll hög kvalitet och var klara i tid."

  • Industri Finansiella tjänster
  • Teamstorlek 2 specialister
  • Varaktighet 8 månader
  • Tjänster IT-hanterade tjänster
Gian Luca De Bonis CEO & CTO Enable Development OÜ
företagets logotyp

"Vi är imponerade av deras flexibilitet och vilja att hitta lösningar på utmanande situationer. De har aktivt hjälpt till i alla typer av situationer. Teamets vilja att leverera optimala resultat säkerställer att partnerskapet blir framgångsrikt."

  • Industri IT-konsult
  • Teamstorlek 8 specialister
  • Varaktighet 36 månader
  • Tjänster Förstärkning av personalen

FAQ about AI in the pharma industry

How is AI used in pharmaceuticals?

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.

How does AI accelerate drug discovery?

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.

Is AI safe and compliant with pharma regulations?

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

How big is AI in the pharmaceutical industry?

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.

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