Askseek – Your Pharma Sop Conversational Ai Expert
AskSEEK simplifies SOPs with AI-powered, role-specific guidance and real-time compliance tracking—helping teams work efficiently and stay audit-ready.
Backed By Purpose. Built For Impact
Convert dense, complicated procedures into clear, easy-to-follow instructions tailored to specific roles.
Access expert assistance anytime, boosting productivity around the clock.
Receive instant, AI-powered answers to SOP-related queries, ensuring accurate execution every time.
Automate adherence to regulatory standards with up-to-date guidance to tracking employee interactions.
Easily connect AskSEEK with ERP, LMS, or document management platforms for streamlined operations.
Enhance accessibility and clarity with robust language support across diverse regions.
Designed With Features That Drive Real Impact
Engage naturally with AskSEEK to clarify SOP details without navigating lengthy documents.
What can i help you with?
Stay updated on policy changes, procedural adjustments, and compliance requirements.
Deliver personalized SOP guidance based on job function, location, and specific regulatory needs.
Automatically record interactions and confirmations to simplify regulatory audits and training initiatives.
Explore How Askseek Is Applied Across Real-world Pharma Workflows.
Accelerate new employee integration using interactive SOPs that ensure consistent and effective training.
Maintain excellence at every stage of production with standardized procedures that uphold high-quality standards.
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.
All your data is encrypted, both in transit and at rest.
Control who sees what with customizable role-based access.
Every action is logged automatically to support traceability and accountability.
21 CFR Part 11 Ready
Supports electronic records and signatures to meet FDA requirements.
Generate audit-ready logs without manual work.
Stay on top of changes with real-time updates and reminders.
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.