FlowForma's AI-powered Process Automation platform integrates forms, workflow, analytics, and document generation. It's powerful platform is proven to help organizations rapidly build out their digital processes with intelligent workflow automation, resulting in increased visibility, productivity and efficiency.
FlowForma ensures secure, compliant process automation for Pharma and Life Sciences. Built on SharePoint, it keeps data protected with audit trails, access controls, and retention policies, supporting regulatory compliance while keeping SharePoint as the single source of truth.
Whether it’s new employees, contract research organizations (CROs), suppliers, or manufacturing partners, onboarding in pharma and life sciences is highly regulated and documentation-heavy. By automating onboarding workflows, organizations can standardize processes, reduce manual errors, and ensure all required documentation, training, and approvals are completed efficiently and compliantly.
Regulatory compliance is at the core of pharma and life sciences operations, from GxP and FDA requirements to EMA and MHRA regulations. FlowForma’s no-code automation platform provides built-in audit trails, version control, and traceability, ensuring every step of a process is fully documented. This makes inspections, audits, and compliance reporting simpler, faster, and more reliable.
Approval processes for deviations, CAPAs, change controls, batch records, and SOPs are critical but often slow and fragmented. FlowForma’s AI-powered Copilot enables teams to quickly create compliant, role-based approval workflows that align with internal quality systems—reducing delays while maintaining full oversight and control.
Managing change in regulated environments requires strict control and documentation. FlowForma streamlines change control, deviation management, and CAPA workflows, ensuring all changes are reviewed, approved, and implemented in line with quality and regulatory requirements—while providing complete visibility and traceability across the organization.
From study start-up activities and site approvals to protocol amendments and document reviews, clinical and research processes involve multiple stakeholders and complex workflows. FlowForma digitizes and automates these processes, reducing administrative burden, improving collaboration, and helping teams focus on accelerating research outcomes.
Preparing for internal audits, supplier audits, and regulatory inspections can be time-consuming and stressful. FlowForma simplifies audit management by automating audit workflows, capturing evidence, tracking findings, and ensuring timely corrective actions—providing confidence and readiness at all times.
Transform your business processes with smarter, faster automation.
Try our all-in-one platform for free below.
From pharmacovigilance to change control to release approvals, FlowForma accelerates the digitization of your critical workflows, eliminating manual bottlenecks and freeing your teams to focus on quality, innovation, and outcomes.
Stay inspection-ready with complete audit trails, role-based approvals, signed activities, and traceable workflow histories that support GxP, FDA 21 CFR Part 11, EMA, and other life sciences regulatory frameworks.
AI agents automate data validation, extract key information from forms, and help guide decisions, reducing errors and speeding up complex quality and compliance processes, while built-in analytics delivers real-time visibility for better decisions.
Drive accountability and visibility across departments involved in artwork approvals, supplier qualification, pharmacovigilance, and innovation processes, ensuring every step is completed, tracked, and transparent.
Gain real-time performance dashboards and process insights to identify bottlenecks, optimize workloads, and support risk-based decision-making, helping you accelerate product launch timelines and reduce operational risk.
FlowForma is built natively on Microsoft SharePoint, allowing pharma and life sciences organizations to keep all process data, documents, and audit trails securely within their own Microsoft 365 tenant. This ensures full data ownership, enterprise-grade security, and alignment with existing identity, access controls, and validation frameworks.
Head of Internal Audit & Compliance, Vestergaard
Contracts Process Transformed With Automation
“It was very difficult and time consuming establishing the status of a particular contract, so there was clearly a need to have an automated.
The efficiency it has brought to the operational part of managing a contract has been very important. It’s a fantastic tool.”
Head of Digital Identity,
Blackpool Teaching Hospital NHS
55 Processes Automated In Year 1
"The speed of development and the opportunity to involve process owners in creating their own FlowForma forms and workflows is a game-changer. The ability to create workflows quickly with governance from IT, without being reliant on them, is critical. "
FlowForma is an AI-powered process automation platform that enables pharmaceutical and life sciences organizations to rapidly automate complex business processes, improving visibility, productivity, and compliance while reducing manual effort.
FlowForma is built as a no‑code process automation platform that runs natively within your organisation’s Microsoft 365 and SharePoint environment, leveraging the familiar Microsoft collaboration stack. This enables seamless integration with SharePoint, Teams, Outlook, and other Office 365 tools, while providing enterprise‑ready forms, workflows, analytics, and document generation all in one place.
With FlowForma, all process‑related data — including forms, documents, and workflow records — is stored within your own SharePoint Online or Microsoft Azure tenancy, under your organisation’s governance and security policies. This means you retain full control over data residency, access rights, and compliance. Data in transit is encrypted, and the solution inherits Microsoft’s enterprise‑grade security controls such as role‑based access and audit logs.
While FlowForma can automate any business process, some of the most in demand workflows include artwork approvals, pharmacovigilance case management, compliance workflows, collaborative review cycles, and performance reporting across departments.
The platform embeds audit trails, e‑signatures, and historical tracking into workflows, making it easier to demonstrate compliance with regulatory requirements and prepare for internal or external audits.
Yes, FlowForma enables cross‑functional collaboration by managing shared workflows and data access, ensuring all stakeholders can contribute and approve steps in a controlled and transparent manner.
Pharmacovigilance is the process of monitoring drug safety and adverse reactions. FlowForma captures pharmacovigilance signals, logs each step in the review cycle, and maintains a secure, auditable record of actions taken and decisions made.
Yes. FlowForma’s automation includes document generation and version control, helping standardise documents used in artwork, clinical, and quality management processes while reducing errors from manual handling.
FlowForma provides real‑time dashboards and analytics that show process status, bottlenecks, and performance metrics — empowering decision‑makers with actionable insights.
Yes — organisations use FlowForma to formalise innovation processes, tracking the lifecycle from idea generation through review, approval, and eventual product launch.
Absolutely, FlowForma is designed to meet the needs of global operations, supporting complex, multi‑stage processes with rigorous audit controls and compliance documentation, which is essential for regulated pharmaceutical environments.