CONGA FOR LIFE SCIENCES AUTOMATION SOLUTIONS
Accelerate the Path from Clinical Innovation to Commercial Impact
Conga replaces manual handoffs with unified life sciences workflow automation, enabling clinical trial contracting and market access, bringing therapies to patients faster.
Trusted by global leaders in medical devices and pharmaceuticals
Master the Complexity of Life Sciences Business Processes
Replace manual bottlenecks with connected life sciences automation solutions that align clinical, commercial, and legal teams to drive improved patient care.
Fast-track clinical trial contracting
Standardize site agreements and accelerate investigator onboarding to gain approvals and reach patients faster.
Optimize commercial pricing and contracting
Execute complex government, payer, and provider contracts delivering tiered and formulary pricing.
Simplify patient and provider communications
Generate compliant patient access materials and field-force documents at scale to improve therapy adherence.
One Platform for Every Life Sciences Workflow
Conga connects pricing, contracting, and document automation within a single operating model to automate life sciences business processes from clinical development through commercialization.
Optimize pricing with AI-driven precision
Set precise, account-specific pricing across complex global portfolios while protecting margins and commercial flow.
Connect revenue and commerce workflows end-to-end
With CPQ for life sciences, quoting and commercial approvals to automate complex product, service, and rebate workflows.
Centralize every regulated agreement lifecycle
Orchestrate pharma contract lifecycle management, market access agreements, and clinical contracts on one CLM.
Automate compliant document delivery
Centralize life sciences document management with automated generation, routing, and eSignature across regulated workflows.
Decreased time spent developing weekly sales forecast presentations
Conga Composer
We love Conga. We leverage their solutions in many of our business processes. Very powerful!
Increased efficiency and time savings across both the sales and legal teams
Conga CLM
Conga CPQ
We're generating new insights about the agreements that are in process, how long it takes to generate them, and the volume of activity. That's been especially useful for the legal side of things.
Improved compliance and value creation
Conga CLM
The real value is that we will provide our business owners of these contracts really accurate data. And moving forward, we will have a better sense of our contracting universe.
Ready to optimize your life sciences operations?
Discover how Conga delivers configured automation for life sciences to simplify regulated workflows, improve compliance, and accelerate execution from clinical trials to commercialization.
Frequently asked questions
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Who are the top CPQ platforms for healthcare and life sciences?
The top CPQ platforms for healthcare and life sciences handle complex product configurations, multi-tier pricing, and regulated approval workflows. Conga CPQ for life sciences manages capital equipment, consumables, software, and service bundles with automated pricing logic, rebate management, and direct CRM and ERP integration.
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Why do I need contract management solutions for life sciences?
You need agreement management solutions because manual processes create compliance gaps, revenue leakage, and operational delays. A life sciences CLM solution gives legal, clinical, and commercial teams one system to standardize contracts, automate approvals, manage contract obligations, and maintain audit-ready records across all deal types.
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What types of contracts are managed in CLM platforms for life sciences?
The agreements managed within contract lifecycle management (CLM) solutions for life sciences organizations include:
- Market access agreements
- Payer and PBM contracts
- GPO and IDN agreements
- Clinical trial site agreements
- Distributor contracts
- Supplier agreements
- Healthcare provider (HCP) engagement contracts
- Patient access documentation
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How does life sciences compliance software mitigate operational risk?
Life sciences compliance software mitigates operational risk by embedding regulatory controls into contracting, pricing, and document workflows. It enforces pre-approved clause libraries, automates approval routing, maintains complete audit trails, and flags non-compliant terms before execution. The result is reduced regulatory exposure across every transaction.
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What are the benefits of automated document management for life sciences?
The benefits of automated document management for life sciences are:
- Faster generation: produce compliant patient, provider, and field sales documents using existing records with one click
- Fewer errors: eliminate version-control issues and inconsistent content across territories via automated data population
- Enforced compliance: secure profitable, compliant, and sustainable growth by embedding regulatory safeguards and validation rules directly into your workflows
- Rapid approvals: route documents to the right stakeholders instantly through integrated eSignatures and automated workflows
- Audit-ready contract compliance: maintain complete records of all document activity for regulatory inspections using centralized tracking
- Scalable delivery: generate and distribute documents individually or in bulk across global teams and patient populations.
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How do life sciences teams collaborate on regulated documents?
Life sciences teams collaborate on regulated documents using centralized platforms that manage version control, approval routing, and contract redlining in a single place. An automated workflow solution like Conga routes documents to legal, clinical, and commercial stakeholders in parallel. With this approach, you shorten review cycles, eliminate email-based handoffs, and maintain a complete audit trail throughout.