Description
Strategic Publication Planning
A comprehensive 2-3 year publication strategy aligned with your clinical development and commercial objectives. GPP 2022-compliant planning sets out which data will be published, when and where, and who will author it — supporting ethical, transparent scientific communication.
Service Details
| Planning horizon | 2-3 years |
| Turnaround | Initial Plan: 6-8 weeks | Annual Update: 3-4 weeks |
| Planning scope | Single product, portfolio, or launch |
| Main deliverable | Comprehensive publication plan document with a publication matrix (Gantt timeline) |
Compliance Framework
- GPP 2022 – Publication planning ethics
- ICMJE – Trial registration and reporting
- COPE – Responsible publication practices
- PhRMA/EFPIA – Industry transparency codes
Publication Plan Components
- Clinical program mapping
- Data availability timeline
- Target journal identification
- Congress strategy
- Author identification and engagement
- Competitive landscape analysis
- Regulatory submission alignment
- Launch timing integration
Deliverables
- Comprehensive publication plan document
- Publication matrix (Gantt timeline)
- Journal target analysis
- Author engagement tracker
- Budget and resource projections
- Risk mitigation strategies
- Quarterly review cadence
Planning Scope
- Single Product: Individual asset publication strategy
- Portfolio: Multiple products/indications
- Launch: Approval-focused publication surge
How It Works
- Share your clinical development program, available and expected data, and commercial objectives
- We map the clinical program and competitive landscape and identify target journals, congresses and authors
- You review the draft publication plan and we revise it based on your feedback
- You receive the final plan document, publication matrix and supporting trackers, with a quarterly review cadence
Which Service Do You Need?
This service builds the plan. To develop the individual publications in it, see Primary Manuscript Development (Phase 2/3) for pivotal trial results, Secondary & Post-Hoc Analysis Manuscripts for subgroup, exploratory and post-hoc analyses, or Scientific Congress Abstract for congress submissions.
Frequently Asked Questions
What period does the publication plan cover?
A 2-3 year publication strategy, aligned with your clinical development and commercial objectives.
How long does planning take?
The initial plan takes 6-8 weeks. An annual update takes 3-4 weeks.
Can the plan cover more than one product?
Yes. Planning scope can be a single product (individual asset publication strategy), a portfolio (multiple products/indications), or a launch (approval-focused publication surge).
What do we receive?
A comprehensive publication plan document, a publication matrix (Gantt timeline), journal target analysis, an author engagement tracker, budget and resource projections, risk mitigation strategies, and a quarterly review cadence.
Which guidelines and codes does the planning follow?
GPP 2022 publication planning ethics, ICMJE trial registration and reporting, COPE responsible publication practices, and the PhRMA/EFPIA industry transparency codes.
Get started: add this service to your cart, or email co*****@*******se.com to discuss your clinical program and planning scope.
