NIVA's biotechnology AI chatbot handles research protocol queries, reagent and equipment information, regulatory submission support, clinical pipeline enquiries, and licensing queries · accelerating biotech operations from bench to market.
BioBot
Biotechnology support · online
Powered by NIVA
NIVA handles the scientific service queries, regulatory information requests, and licensing enquiries that consume specialist team time · so scientists and BD teams focus on discovery and deals.
Scientists query available research services · gene editing, protein expression, assay development, and animal model services · through chat. NIVA provides accurate service descriptions and routes feasibility calls to the right scientific team.
Researchers query reagent specifications, lot-specific Certificates of Analysis, storage requirements, and compatibility information through chat. NIVA retrieves documents from your product information system instantly.
Regulatory teams query EMA/FDA guidance document interpretations, IND/CTA submission requirements, GMP compliance, and orphan designation criteria through chat · from your approved regulatory documentation library.
Licensing & Partnering Enquiries
Partners and pharma companies query technology licensing terms, co-development structures, and pipeline partnership opportunities through chat. NIVA qualifies the interest and routes to the correct BD director.
Clinical Pipeline Queries
Investors and partners query clinical trial status, therapeutic area focus, and IND milestone progress through chat. NIVA provides approved pipeline information from your investor relations content.
Investor Relations & Media
Investors and journalists query financial data, patent portfolio status, and corporate development milestones through chat. NIVA provides approved IR content and routes media enquiries to your communications team.
Examples from live biotechnology deployments, answered in chat instead of routed to inbox.
“What are the current EMA requirements for the Advanced Therapy Medicinal Products (ATMP) classification procedure?”
The ATMP classification procedure is administered by the EMA's CAT (Committee for Advanced Therapies). For classification, you submit a scientific data package to the CAT; the procedure takes up to 60 days. ATMPs encompass gene therapy (GTMPs), somatic cell therapy (sCTMPs), and tissue-engineered products (TEPs). Combined ATMPs (medical devices + ATMPs) require additional assessment. Classification is voluntary but highly recommended before IND/CTA filing. I can send you the current EMA ATMP classification guidance document and the CAT application form directly. Shall I?
Generic prompts from scratch
250+ industry personas, ready day one
FAQ replies and deflection
Flows, forms, and real actions
Credits, tokens, and add-ons
Flat pricing, full white-label
Teams already using NIVA
From persona selection to live on your biotech company website or partner portal in under a day. NIVA handles enquiries · your scientists focus on discovery.
Choose the Biotechnology vertical from NIVA's library with industry terminology built in.
Pick from 10+ pre-built biotechnology personas. Toggle only the roles you need.
Upload policies, manuals, and FAQs as PDFs or URLs into a private knowledge base.
Drop one script tag on your site. The bot goes live fully branded, no redeploy.
Subscribe to expert roles with domain tone and knowledge already built in. Toggle live without prompt engineering.
Research Services Bot
CRISPR, proteins, assays, animal models
Reagent & Product Bot
CoA, specs, storage, compatibility
Regulatory Affairs Bot
EMA/FDA, IND/CTA, GMP, orphan
Licensing & BD Bot
Tech licensing, co-development, pipeline
Pipeline Information Bot
Trial status, milestones, TA focus
Investor Relations Bot
IR queries, patents, corporate milestones
+ 4 more biotechnology personas available on your demo
Platform capabilities tuned for biotechnology teams. Compliance standards are listed separately below.
Upload your service catalogues, regulatory guidance interpretations, CoA libraries, and pipeline publications. NIVA answers technical and regulatory queries from your approved scientific documentation.
NIVA tracks each partner's active collaborations, technology enquiries, and CDA status · giving BD and scientific teams full context on every partner relationship.
Build service enquiry qualification flows and licensing BD routing workflows. Trigger CRM opportunity creation and scientific feasibility review assignments automatically.
NIVA integrates with Veeva, Salesforce Life Sciences, and custom LIMS and pipeline management systems. Scientific data, partner records, and pipeline status sync automatically.
Service Enquiry to Feasibility Flow
Trigger
Scientist enquires about CRISPR service
Qualify
Model, construct type, timeline needs
Route
Service docs sent, feasibility call booked
CRM
Lead captured, scientist team notified
Workflows, smart forms, and multi-persona routing from a single admin dashboard.
Build multi-step automated workflows inside the chat: conditional branching, dynamic forms, persona handoffs, and webhook triggers.
Learn more Smart FormsDefine unlimited forms per bot. The AI reads conversation context and surfaces the right form automatically, inline in the widget.
Learn more Multi-Persona AIRun multiple AI agents in one widget. The orchestrator routes each message to the right persona automatically.
Learn moreDrop a single line before </body> and your biotechnology bot goes live, fully branded as BioBot.
Auto-branded
Your colours, avatar, and bot name in every channel.
Instantly updated
Change personas or flows in admin. No redeploy.
CORS-ready
Website, WhatsApp, and custom domains out of the box.
Book a 30-minute demo and see NIVA's biotechnology personas handling service enquiries, regulatory queries, and licensing discussions live.
Quick answers before you book a demo.
Still unsure? Send us your requirements and we will map the right personas for biotechnology.
See how NIVA handles specific workflows in your space.
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