Life Sciences & Pharmaceuticals

Third-Party Due Diligence & Compliance Case Management

Manage regulated third-party due diligence through screening, reviewer routing, certification and auditable case closure.

The solution automated multiple anti-corruption and due-diligence processes for a global pharmaceutical group using a reusable case-management model. Source material covers Standard Due Diligence, HCP Sponsorship, HCP Assessment, Medical Research Due Diligence, Grants & Donations and Small Unsolicited Donations.

Life Sciences & Pharmaceuticals Governance & Enterprise Decision Management Microsoft 365 & SharePoint Workflow & Automation Enterprise Applications & Integration

Business challenge

  • Different due-diligence processes required consistent case handling and reusable workflow patterns.
  • External-party data, screening results and reviewer decisions needed to remain tied to one case lifecycle.
  • Compliance, legal, management and affiliate roles required controlled routing, worklists and case history.

Para approach

  1. Initiate a case and assign a persistent case ID.
  2. Capture external-party and service context.
  3. Run validation and restricted-party screening.
  4. Collect questionnaires, certifications and supporting artifacts.
  5. Route review through compliance, legal, management and other required roles.
  6. Close the case with generated certification, status history and audit evidence.

How it works

Source-grounded due-diligence case-management lifecycle. Evidence: solution design specification, K2 technical design and mockups covering standard due diligence, HCP, medical research due diligence, grants and donations, screening, review, case history and certification.

1

Case Initiation

2

Validation / RPS Screening

3

Questionnaire / Artifacts

4

Compliance Review

5

Legal / Management Review

6

Certification / Closure

Delivered capability

Reusable case management

Common case ID and lifecycle across multiple due-diligence processes.

Validation & screening

Certification validation, restricted-party screening and batch or full external search.

External party interaction

External questionnaires and artifact submission.

Role-based review

Compliance, legal, management and HCP or secondary reviewer paths.

Case worklists & history

Assigned tasks, case status and historical actions.

Certification & audit

Generated certification documents, close status, archival metadata and reporting.

Evidence-supported outcomes

Controlled case lifecycle

A consistent path from initiation through screening, review, certification and closure.

Reviewer accountability

Clear routing and case or worklist visibility across responsible roles.

Reusable compliance pattern

Common case management supports several regulated processes.

Traceable evidence

Case history, generated documents and reporting support audit-oriented operations.

Technology & delivery context

Historical K2 workflow, ASP.NET workflow and external-party forms, a SharePoint portal and libraries, SQL data stores and generated certification documents using OpenXML. This is a historical case; it does not describe current product packaging or a current technology baseline.

Have a similar enterprise challenge?

Para can assess the current state, define the business and information model, shape the architecture and delivery approach, and move from business need into implementation and ongoing operations.

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