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Publive supports the strict content governance requirements of the pharmaceutical and healthcare industry.

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Regulatory Requirements

RequirementPublive Feature
Multi-step review processStatus workflow: Draft → Approval Pending → Published
Content traceabilityFull audit trail with member, approver, updated_by fields
Version controlDraft/Published state separation
Access restrictionsAPI key isolation, access_type metadata
Scheduled publishingScheduled status with scheduled_at datetime

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Implementation Pattern

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1. Content Creation (Medical Writer)

curl -X POST \
  'https://cms.thepublive.com/publisher/123/post/' \
  -H 'Content-Type: application/json' \
  -d '{
    "title": "Drug Safety Update - Product XYZ",
    "english_title": "Drug Safety Update - Product XYZ",
    "type": "Article",
    "status": "Draft",
    "primary_category": 300,
    "content": "<p>Updated safety information for Product XYZ...</p>",
    "meta_data": {"access_type": "Paid", "compliance_level": "restricted"}
  }'

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2. Medical Review (Submit for Approval)

curl -X PATCH \
  'https://cms.thepublive.com/publisher/123/post/{id}/' \
  -H 'Content-Type: application/json' \
  -d '{"status": "Approval Pending"}'

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3. Regulatory Approval (Compliance Officer)

curl -X PATCH \
  'https://cms.thepublive.com/publisher/123/post/{id}/' \
  -H 'Content-Type: application/json' \
  -d '{"status": "Published"}'

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Content Organization

Recommended category structure for pharma:
CategoryPurpose
Drug SafetySafety updates and alerts
Clinical TrialsTrial results and publications
Regulatory UpdatesCompliance and regulatory changes
Patient InformationPublic-facing health content
Internal CommunicationsStaff-only content

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Best Practices

  1. Enforce Approval Pending for all content before publication
  2. Use meta_data to tag compliance classifications
  3. Maintain separate API keys for writers, reviewers, and publishers
  4. Use scheduled_at for coordinated release of regulatory content
  5. Track seo_keyphrase for medical terminology accuracy