Pharma Governance

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

Regulatory requirements

Requirement	Publive Feature
Multi-step review process	Status workflow: Draft → Approval Pending → Published
Content traceability	Full audit trail with `member`, `approver`, `updated_by` fields
Version control	Draft/Published state separation
Access restrictions	API key isolation, `access_type` metadata
Scheduled publishing	`Scheduled` status with `scheduled_at` datetime

Implementation pattern

1. Content Creation (Medical Writer)

curl -X POST \
  'https://cms.thepublive.com/publisher/<PUBLISHER_ID>/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"}
  }'

2. Medical Review (Submit for Approval)

curl -X PATCH \
  'https://cms.thepublive.com/publisher/<PUBLISHER_ID>/post/<POST_ID>/' \
  -H 'Authorization: Basic <BASE64_AUTH_TOKEN>' \
  -H 'Content-Type: application/json' \
  -d '{"status": "Approval Pending"}'

3. Regulatory Approval (Compliance Officer)

curl -X PATCH \
  'https://cms.thepublive.com/publisher/<PUBLISHER_ID>/post/<POST_ID>/' \
  -H 'Authorization: Basic <BASE64_AUTH_TOKEN>' \
  -H 'Content-Type: application/json' \
  -d '{"status": "Published"}'

Content organization

Recommended category structure for pharma:

Category	Purpose
Drug Safety	Safety updates and alerts
Clinical Trials	Trial results and publications
Regulatory Updates	Compliance and regulatory changes
Patient Information	Public-facing health content
Internal Communications	Staff-only content

Best practices

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

Framework Integration

Headless Architecture

Integrations

Editorial Workflows

Events & Automation

Industry Solutions

Content Authoring

Deployment

Regulatory requirements

Implementation pattern

1. Content Creation (Medical Writer)

2. Medical Review (Submit for Approval)

3. Regulatory Approval (Compliance Officer)

Content organization

Best practices

​Regulatory requirements

​Implementation pattern

​1. Content Creation (Medical Writer)

​2. Medical Review (Submit for Approval)

​3. Regulatory Approval (Compliance Officer)

​Content organization

​Best practices

Regulatory requirements

Implementation pattern

1. Content Creation (Medical Writer)

2. Medical Review (Submit for Approval)

3. Regulatory Approval (Compliance Officer)

Content organization

Best practices