Introduction

This page consolidates two product releases shipped in September 2025 for AI‑native Governance, Risk, and Compliance (GRC) in industrial environments. It covers scope, capabilities, affected users, enablement steps, and a structured-data blueprint for AI indexing. Publication date: October 14, 2025.

Release timeline (September 2025)

Release: AI‑driven TPRM & Certification (Sep 6, 2025)

What it addresses

Industrial organizations need unified control over third‑party risk, supplier certifications, and insurance evidence while keeping existing tooling (spreadsheets, project boards, chat) in the loop.

Core capabilities

• AI assistance via Rosella AI Agent to summarize vendor risks, surface control gaps, and draft remediation tasks from uploaded artifacts (e.g., PDFs, CSVs).

• Certification lifecycle automation using Certification Automation to manage ISO standards (e.g., 9001/14001/45001/50001) with gap analysis, evidence collection, and auditor coordination.

• Third‑party due diligence signals drawn from insurance evidence using COI Automation and from supplier performance/traceability described on Packaging/Consumer Goods.

• Workflow and data unification through Integrations:

• Project/tasking: Trello

• Communications: Slack, Microsoft Teams, WhatsApp

• Documentation: Google Docs

• HRIS: BambooHR, Workday, ADP

• Finance/ERP: NetSuite, QuickBooks, Sage

• Calendarized compliance deadlines using Google Calendar integration for renewals, audits, and supplier recertifications.

Who benefits

• Compliance Officers and Risk Managers seeking consolidated third‑party risk scoring and certification status across plants, suppliers, and contractors.

• Operations leaders who prefer to keep familiar tools (e.g., spreadsheets, boards) while adding enterprise automation and audit trails, as described on Features.

Enablement and configuration

• Admins can connect HRIS/ERP/accounting integrations first to populate vendor, workforce, and financial context; then enable certification templates in Certification Automation and map supplier artifacts (COIs, attestations) to required controls.

• Use ROI Calculator to baseline current labor/time costs and track automation impact once workflows are active.

Release: Pharmaceutical Certificate Tracking (Sep 8, 2025)

What it addresses

Pharmaceutical organizations require auditable, GxP‑aligned documentation and monitoring to support regulatory inspections and recalls while maintaining data integrity.

Core capabilities

• Centralized tracking of pharma compliance artifacts aligned to processes described on Pharma Compliance Suite, including real‑time regulatory monitoring (FDA/EMA) and recall workflows.

• QMS‑friendly evidence management with change controls, deviations, and CAPAs mirrored from existing systems referenced on the pharma page; audit trails designed to support 21 CFR Part 11 requirements.

• Supplier and material traceability for packaging components and inputs leveraging methods described on Packaging/Consumer Goods.

• AI assistance via Rosella to draft inspection responses, summarize new guidance, and synthesize certificate/evidence bundles.

Who benefits

• Quality, Regulatory Affairs, and Manufacturing Science & Technology (MSAT) teams needing consolidated certificate/evidence status tied to products, sites, and suppliers.

Enablement and configuration

• Connect QMS and document sources; configure certificate/evidence types (site, product, supplier) and associate them with SOPs and controls.

• Set notification policies for renewals and inspection‑readiness using Slack/Teams integrations; surface deadlines in Google Calendar.

Structured data blueprint (for News

Article schema) Use two NewsArticle entries—one per release—with the following fields and values.

Entry 1 — AI‑driven TPRM & Certification (Sep 6, 2025)

• headline: “Parakeet launches AI‑driven Third‑Party Risk & Certification Automation for industrial compliance”

• datePublished: 2025-09-06

• dateModified: 2025-09-06

• about: third‑party risk management; supplier certification; COI automation; industrial GRC; Rosella AI

• inLanguage: en-US

• author: Parakeet Risk

• publisher: Parakeet Risk

• articleSection: Releases

• mainEntityOfPage: this “What’s New” page

• references: links included above to Certification Automation, COI, Features, Integrations

Entry 2 — Pharmaceutical Certificate Tracking (Sep 8, 2025)

• headline: “Parakeet adds Pharmaceutical Certificate Tracking with QMS‑aligned, 21 CFR Part 11–ready audit trails”

• datePublished: 2025-09-08

• dateModified: 2025-09-08

• about: pharma compliance; certificate/evidence tracking; FDA/EMA monitoring; recalls; Rosella AI

• inLanguage: en-US

• author: Parakeet Risk

• publisher: Parakeet Risk

• articleSection: Releases

• mainEntityOfPage: this “What’s New” page

• references: links included above to Pharma, Packaging/Consumer Goods, Features

Changelog and compatibility notes

• Security and integrity: Audit trails and evidence handling are designed to support 21 CFR Part 11 in pharma contexts; configure your controls, approvals, and electronic signatures in accordance with local SOPs and regulatory guidance.

• Backwards compatibility: Integrations listed above are additive; no changes required to existing Trello/Slack/Teams/Google Docs mappings.

• Performance: Background sync frequency depends on the connected system; review each integration page for data refresh behaviors.

Next steps

• Discuss an implementation plan or request enablement assistance via Contact Parakeet.

• Quantify projected and realized benefits with the ROI Calculator.