Platform

Services

Technology

Resources

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Platform

Services

Technology

Resources

Book a demo

PLATFORM

AI Workflows for Life Sciences.

Everest combines regulatory structure and domain expertise to take you from source files to submission-ready, in minutes.

Book a demo

PLATFORM

AI Workflows for Life Sciences.

Everest combines regulatory structure and domain expertise to take you from source files to submission-ready, in minutes.

Book a demo

PLATFORM

AI Workflows for Life Sciences.

Everest combines regulatory structure and domain expertise to take you from source files to submission-ready, in minutes.

Book a demo

The document you need.
Straight from your data.

Start with a prompt and your source data. Everest builds the workflow around how your team actually works — generating intermediate reports with built-in QC and final validation.

Not just the document.
The statistics underneath it.

Everest doesn't stop at the document — it builds the analysis underneath it. Here, that means generating a CSR's TLFs and the R and SAS code to reproduce them: the role of a biostatistician, performed in minutes.

Clinical trials

Clinical Trial Documentation

Turn your protocol into structured, reusable documentation across the clinical trial lifecycle.

“After 20 years of writing imaging documents manually, we know exactly where the inefficiencies are. With Everest, our team now focuses on higher-value scientific work.”

Ashley Ferreira, CEO

Study protocols & amendments

Clinical Study Reports (CSRs)

Investigator Brochures (IBs)

Statistical Analysis Plans (SAPs)

Safety narratives & listings

Trial master file (TMF) documentation

Clinical summaries & supporting documents

Health Authority responses

INDs & IND amendments

NDAs / BLAs (partial or full)

Clinical Study Reports (CSRs)

Investigator Brochures (IBs)

Quality Overall Summaries (QOS)

Nonclinical & clinical summaries

Regulatory briefing documents

Health Authority responses & supplements

Pharma/biotech

eCTD Modules 1-5

Produce FDA-aligned INDs, NDAs, and BLAs faster — without sacrificing rigor or control.

medtech

MedTech Regulatory Documentation

Produce review-ready MedTech regulatory documentation faster, with built-in traceability.

“Everest cut our literature screening time by up to 50% — with no compromise on the accuracy or compliance our work demands.”

Mark G. Grondin, CEO

510(k) submissions & updates

Clinical Evaluation Reports (CERs)

Clinical Evaluation Plans (CEPs)

State of the Art (SOTA) reviews

Predicate device comparisons

Regulatory responses & supplements

Business Plan

Product Requirements Document (PRD)

Reimbursement Strategy Brief

Competitive Analysis

Market Landscape Summary

Scientific Literature Review

Business & Product Strategy

Commercial and Strategic Documents

From business plans to reimbursement strategies, the same Everest delivers decision-ready drafts — grounded in your data.

Clinical Trials

Every phase.
Every deliverable.

From working reports through clinical documents to complete regulatory submissions.

Beyond clinical trials: explore solutions for pharma/biotech, medtech, and business strategy.

study startup

Protocol

Investigator Brochures (IB)

Patient Consent Form

Investigational New Drug Application (IND)

study conduct

Protocol Amendments

Operational Documents

Safety Reports

Eligibility Package

submission

Strategic/Commercial

Patient Narratives

Clinical Study Reports (CSRs)

Clinical Summaries

New Drug Application (NDA)

“Everest cut our literature screening time by up to 50% — with no compromise on the accuracy or compliance our work demands.”

Mark G. Grondin, CEO

“After 20 years of writing imaging documents manually, we know exactly where the inefficiencies are. With Everest, our team now focuses on higher-value scientific work.”

Ashley Ferreira, CEO

“Finalizing a CER used to take weeks of back-and-forth across regulatory, clinical, and quality teams. With Everest, we had a near-final draft in under an hour.”

Regulatory Affairs Consultant

EU MDR-Compliant MedTech Company

A platform you can trust

Everest gives you full data control with built-in enterprise-grade security—so your team can focus on results, not risk.

Data ownership

All templates, files, and outputs are customer-owned and isolated per account. Everest never shares, sells, or accesses your content without your consent, so you know your data is safe.

Data privacy

We implement strict privacy controls, including customizable anonymization and retention policies. There is zero data retention with LLM providers such as OpenAI, Anthropic, and AWS Bedrock.

Data security

Everest is fully SOC 2 Type II and HIPAA compliant, with enterprise-grade security built on AWS and validated through independent audits. Enterprise teams can enable optional features like VPC deployment and enhanced data isolation for greater control and protection.

A platform you can trust.

Everest gives you full data control with built-in enterprise-grade security—so your team can focus on results, not risk.

Data ownership

All templates, files, and outputs are customer-owned and isolated per account. Everest never shares, sells, or accesses your content without your consent, so you know your data is safe.

Data privacy

We implement strict privacy controls, including customizable anonymization and retention policies. There is zero data retention with LLM providers such as OpenAI, Anthropic, and AWS Bedrock.

Data security

A platform you can trust.

Everest gives you full data control with built-in enterprise-grade security—so your team can focus on results, not risk.

Data ownership

All templates, files, and outputs are customer-owned and isolated per account. Everest never shares, sells, or accesses your content without your consent, so you know your data is safe.

Data privacy

We implement strict privacy controls, including customizable anonymization and retention policies. There is zero data retention with LLM providers such as OpenAI, Anthropic, and AWS Bedrock.