SEEK

AskSEEK – AI SOP Assistant Built for Pharma

AskSEEK is an AI-powered SOP assistant designed for pharma teams. It delivers instant,
role-based answers from approved SOPs, streamlining compliance, reducing human error, and ensuring audit readiness on the shopfloor.

Backed by purpose. Built for impact

AI-Driven SOP Simplification

Convert dense, complicated procedures into clear, easy-to-follow instructions tailored to specific roles.

Real-Time Guidance

Receive instant, AI-powered answers to SOP-related queries, ensuring accurate execution every time.

Automated Reg - Compliance

Automate adherence to regulatory standards with up-to-date guidance to tracking employee interactions.

24/7 AI Support

Access expert assistance anytime, boosting productivity around the clock.

Seamless Integration

Easily connect AskSEEK with ERP, LMS, or document management platforms for streamlined operations.

Multilingual Capabilities

Enhance accessibility and clarity with robust language support across diverse regions.

KEY FEATURES

Designed with features that drive real impact

Conversational AI Interface

Engage naturally with AskSEEK to clarify SOP details without navigating lengthy documents

Real-Time Alerts & Notifications

Stay updated on policy changes, procedural adjustments, and compliance requirements

Role-Based Access Control

Deliver personalized SOP guidance based on job function, location, and specific regulatory needs

Audit-Ready Compliance Logs

Automatically record interactions and confirmations to simplify regulatory audits and training initiatives

Practical applications

Explore how AskSEEK is applied
across real-world pharma workflows

Compliance Management

Navigate complex regulations effortlessly with reliable SOP guidance

Onboarding Optimization

Accelerate new employee integration using interactive SOPs that
ensure consistent and effective training

Quality Control Assurance

Maintain excellence at every stage of production with standardized
procedures that uphold high-quality standards

Experience AskSEEK in Action

Ready to transform your SOP process? Request a free demo today and unlock the full potential of AI-powered SOP assistance. Our team is here to support you every step of the way

Built for Safety, Designed for Trust

At AskSEEK, we understand the importance of protecting your data and meeting strict industry regulations
like those from the FDA. Our platform is built with advanced security features and compliance tools that
keep your information safe while helping you meet regulatory standards with ease

Secure by Design

Data Encryption

All your data is encrypted, both in transit and at rest

Access Controls

Control who sees what with customizable role-based access

Audit Trails

Every action is logged automatically to support traceability and accountability

FDA Compliance Made Simple

21 CFR Part 11 Ready

Supports electronic records and signatures to meet FDA requirements

Automated Documentation

Generate audit-ready logs without manual work

SOP Tracking & Alerts

Stay on top of changes with real-time updates and reminders

Whether you are in pharmaceuticals, biotech, or healthcare, AskSEEK ensures your team
works within a secure, compliant environment every step of the way

FAQ

Is AskSEEK compliant with FDA 21 CFR Part 11 requirements?

Yes, AskSEEK fully supports 21 CFR Part 11, including secure user authentication, electronic signatures, and complete audit trails.

Can AskSEEK help us standardize and control our SOPs across multiple sites?

Absolutely. AskSEEK allows you to centralize SOPs, customize them by role or location, and ensure consistency across all facilities.

How does AskSEEK assist with audit readiness?

AskSEEK automatically logs user interactions, SOP confirmations, and compliance activities—making audit prep faster and stress-free.

Can the platform be integrated with our existing LIMS or QMS?

Yes, AskSEEK offers seamless integration with major enterprise systems including LIMS, QMS, ERP, and document management platforms.

Does AskSEEK support multilingual SOPs for global teams?

Yes, AskSEEK offers robust multilingual support, helping global QC teams access clear and compliant SOP guidance in their preferred language.

Can AskSEEK track deviations or non-conformances during SOP execution?

Yes, AskSEEK can flag deviations automatically and log them for review, ensuring that any non-conformances are tracked, addressed, and documented for audit purposes.

Is AskSEEK suitable for Quality Control labs in the pharmaceutical industry?Absolutely.

AskSEEK simplifies lab SOPs, provides step-by-step role-specific guidance, and helps QC teams follow exact procedures—reducing human error and improving documentation accuracy.

How does AskSEEK support training and onboarding of new QC analysts?

AskSEEK offers interactive SOPs, real-time assistance, and multilingual support that accelerate onboarding and ensure consistency in training across batches of new hires.

Can AskSEEK integrate with our existing LIMS or Document Management System?

Yes, AskSEEK is designed to seamlessly integrate with systems like LIMS, ERP, and document control platforms, ensuring smooth data flow and centralized operations.