Services

Integrated scientific communications, built around your needs

SciVoc delivers end-to-end support across medical affairs assets, medical communications, HEOR and RWE, regulatory writing, patient engagement, and digital scientific content. Whether you need a strategic partner, overflow support, or urgent-response execution, SciVoc adapts to your team's requirements and timelines.

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Services

End-to-end support across the drug development lifecycle

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01Medical AffairsScientific exchange and field-team enablement
ONE STATEMENTCONSISTENT EXCHANGE

Agreed scientific statements

MEDICAL AFFAIRS
FIELD
MSL training decks, response letters, and standard-response documentsAdvisory board materials, from pre-reads to post-meeting reportsCompetitive intelligence: treatment-landscape updates, pre- and post-congress reports, monthly literature monitoring
02Medical CommunicationsPublication and communication strategy across the product lifecycle
CONGRESSJOURNALINTERNALQ1Q2Q3Q4Q5ABSTRACTPOSTERMANUSCRIPTPLATFORM

Congress dates and Journal windows

ABSTRACT
MANUSCRIPT
Scientific communication platform development — the layer that governs every downstream assetPublication planning and management across congress and journal calendarsGuidelines and recommendations, consensus documents, position papers, book chapters
03HEOR and RWE CommunicationsComplex evidence, translated into value stories
INCREMENTAL EFFECTINCREMENTAL COSTWILLINGNESS TO PAY95% CI

Model output is a cloud

Δ EFFECT
Δ COST
Systematic and targeted literature reviews, and real-world evidence protocolsBudget-impact and cost-effectiveness models written up for publication and HTAValue dossiers, HTA sections, and burden-of-illness narratives
04Regulatory WritingSubmission-focused writing with scientific precision
M1 · REGIONALM2 · SUMMARIESM3 · QUALITYM4 · NON-CLINICALM5 · CLINICAL2.52.7

Submission is an assembly

MODULE 1
SUBMISSION
CTD Modules 2.5 and 2.7, clinical study reports, protocols and amendmentsDSUR literature search and summary, and pharmacovigilance writing supportInformed consent forms and investigator brochures, QC’d before they reach you
05Patient Engagement CommunicationClarity, empathy, and the patient voice
CLINICAL EVIDENCEPATIENT-REPORTEDHTA · REGULATOR · ADVOCACYACCURACY HELD IN BOTH STRANDS

Clinical evidence has its strand

EVIDENCE
ONE NARRATIVE
Plain-language summaries written down to a target reading grade, not paraphrasedPatient education content and advocacy support materialsHealth-literacy review of existing clinical and corporate content
06Digital SolutionsScientific storytelling built for modern channels
APPROVED EMAILeDETAILERMyINSIGHTSENGAGEAPPROVEDCLAIM

One claim, approved once

APPROVED CLAIM
CHANNELS
Veeva practice: eDetailing and digital sales aids, Approved Email templates and effectiveness review, MyInsights dashboards, content adaptation for Engage2D and 3D medical animation, medical simulation, and audio-visual with voice-overInteractive content authoring for rapid module and microsite buildCreative production and Veeva build are delivered with SciVoc’s extended specialist team.

Rapid response, when timelines turn critical

Last-minute regulatory documents, abstracts, congress materials, publications, overflow deliverables, and time-sensitive scientific content that cannot slip. A rapid brief is escalated on arrival, staffed by a writer with the relevant therapeutic-area background, and reviewed in parallel with drafting — which is how the calendar shortens without a check being skipped. Leadership stays on the file until it lands.

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The services listed here are a sample of what SciVoc delivers. For the full catalog of offerings, get in touch with the SciVoc team.

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Your science has a story worth telling

Tell SciVoc what you are working on, and the team will come back with a tailored approach.

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