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Medical Affairs Services

MSL and Field Medical Materials

Pubrica develops MSL and field medical materials and MSL training for field medical teams. Field medical materials must carry the science accurately, stay within the boundary of scientific exchange and prepare MSLs for questions the materials do not cover. Our field medical writers prepare the core scientific deck, reactive response sets and reference materials, and deliver scenario-based training that prepares MSLs to use them.

  • Built from the scientific platform, so what the field team says matches what the programme supports, and any difference is visible
  • Reactive-use materials marked as reactive, because the distinction between responding to a question and raising a topic defines the boundary
  • Training on difficult questions, including off-label use, comparative efficacy and competitor results that appear stronger than yours
  • Insight capture built into the material, so what the field team hears is returned in a form the organisation can act on
  • Clear examples of the compliance boundary, with worked examples of scientific exchange and promotion rather than a general principle
What field medical support covers What is included and what is excluded

Materials built from the platformIncluded

Reactive and proactive use markedIncluded

Training on unscripted questionsIncluded

Insight capture designed inIncluded

Promotional content for field medicalNot offered

Platform → materials → trained → exchange → insight

Included in every project
  • Built from the scientific platform
  • Reactive use marked as reactive
  • Difficult questions covered in training
  • Insight capture designed in
  • Boundary shown through examples
Quoted per programmeBased on material count and team size
Built from the scientific platformNot from commercial material
Scientific exchangeBoundary defined by example
ISO 9001:2015Quality management certified · cert. H3CR9TCU20251212INDQM10N

Deliverables

Four Components of Every Field Medical Package

Materials are only part of field preparation. MSLs also need training for conversations that go beyond the deck.

Traceable to the scientific platform Every statement in a field deck is traced to the scientific platform and its evidence, so new claims never originate with the field team.

Example from a traceability checkNew claims appear in field materials more often than anywhere else, because decks are built around conversations rather than source documents.

Reactive material marked as reactive Content for responding to unsolicited questions is kept visibly separate from content an MSL may raise, because this distinction keeps scientific exchange non-promotional.

Example from a material setOne deck, all content, use as appropriate.Core scientific deck: may be presented. Reactive response set: used only in response to an unsolicited question on that topic, with the question recorded. Off-label enquiries: routed to medical information, not answered from the deck.

Training on unscripted questions Training covers comparative efficacy where no head-to-head data exist, competitor results that appear stronger, off-label uses the clinician is already trying and requests for unpublished data.

Example from a training programmeCompliance and credibility are both decided in these moments, yet training often skips them in favour of a walkthrough of the materials.

Insight capture designed for action We define what to record and how, so the field team reports specific questions from specific settings rather than general sentiment.

Example from an insight formHCP had concerns about efficacy.Nephrologist, tertiary centre: asks whether the renal-impairment subgroup was pre-specified, because the local formulary committee raised it. Third time this has come up this quarter. That is an evidence gap with a decision attached to it.

The samples shown are illustrative and anonymised. Hover over a sample to replay it.

Compliance and Standards

Field Medical Standards: PhRMA Code, GPP 2022 and ICMJE

Scientific exchange is not promotion, but it is bounded by promotional rules.

Code 2022

PhRMA Code (and the OIG speaker program alert)

The Code revisions effective January 2022 responded directly to the OIG Special Fraud Alert of November 2020. The alert’s suspect characteristics, including minimal educational content, alcohol, unsuitable venues, repeat attendance, sales-influenced speaker selection and compensation above fair market value, define the boundary.

GPP 2022 (good publication practice)

The 2022 update replaces GPP3. It covers company-sponsored research, including translational, biomarker and real-world studies, and extends to preprints, plain language summaries and social media. Professional medical writing support is legitimate, provided it is disclosed.

ICMJE Recommendations (authorship and disclosure)

Sets four criteria, all of which each author must meet. Contributors who do not meet all four are acknowledged. Employment by the sponsor neither qualifies nor disqualifies anyone.

ISO9001:2015

Quality management (cert. H3CR9TCU20251212INDQM10N)

Our certified quality system governs how work is run, recorded and released.

Responsible Use of AI

Our Approach to AI Use in Field Medical Materials

Medical affairs work must distinguish scientific exchange from promotion, a boundary that regulators monitor. That judgement depends on context, jurisdiction and the individuals involved, so it is always made by our specialists rather than by an AI tool.

How We Use AI ToolsWe use AI tools to find published evidence and previously approved material, check terminology for consistency across a plan or a set, summarise a body of literature for a specialist to review, and draft templated sections that a specialist then verifies.
Where We Do Not Use AIWe do not use AI to decide what is scientific exchange and what is promotion, to make authorship or contributorship judgements, to issue responses to healthcare professionals as drafted, or to profile named individuals. Pubrica does not use prescribing data for mapping, and the lawful basis for every data source is documented before work begins.
What Your AI Declaration Should IncludeYour declaration should name the tool, the stage at which it was used and the human oversight applied. Journals, funders, regulators and the ICMJE January 2026 update now expect this, and an undeclared tool found later is treated as an integrity matter.

Why We Do Not Publish AI Accuracy Figures

Accuracy figures for AI tools are usually reported by the companies that sell them.

Pubrica therefore does not quote a self-generated accuracy figure, because it would carry the same conflict of interest. Instead, we tell you which tool was used on your project, at which stage, and what a specialist changed afterwards.

Our Process

How Our Field Medical Process Works

We start with the scientific platform. Materials built before the platform exists tend to become the platform by default.

Step one

Platform and boundary

We confirm the scientific platform as the source and agree the reactive and proactive boundary with medical and compliance teams.

Step two

Materials

We prepare the core scientific deck, reactive response sets and reference materials, each traced to the platform and marked for its permitted use.

Step three

Training

We deliver scenario-based training on unscripted questions, in which MSLs practise the escalation routes.

Step four

Insight capture

We design the capture structure with a route back into the medical plan, so insights lead to action.

Our Experts

Your Field Medical Team

A named team of subject specialists stays with your project from scoping to delivery. Your project coordinator introduces each team member by name before work begins.

Subject matter expertClinical or scientific expert matched to your topic

Reviews the scientific content for accuracy and confirms that each conclusion is supported by the evidence. Each expert is matched to your field.

Responsible forScientific accuracy and interpretation
Reviews againstThe source evidence and current literature
FieldMatched to your topic
Medical writerDrafts content to the applicable code and guidance

Writes the content against the brief and the applicable code of practice, with every claim traceable to its reference.

Responsible forDrafting and source traceability
Reviews againstGPP, ICMJE and the applicable code of practice
OutputReference-annotated content
Medical reviewerScientific and compliance review before delivery

Reviews the content for scientific accuracy, fair balance and compliance with the applicable code before it reaches your internal review.

Responsible forScientific and compliance review
Reviews againstSource data and the applicable code
Signed off byProject lead
Project coordinatorYour single point of contact

Manages the timeline, keeps you informed at each stage and coordinates the team so that questions are answered and deadlines are met.

Responsible forTimeline and communication
Reviews againstYour brief and deadline
OutputDelivery and follow-up

Packages

Field Medical Packages

Costs depend on the number of materials, the size of the field team and the number of markets adapting them.

Materials

Field medical materials

For a field team in one indication

Quoted per projectBased on material count

Delivery Agreed at scoping

  • ✓Core scientific deck from the platform
  • ✓Reactive response sets, marked
  • ✓Reference and back-up slides
  • ✓Every statement traced to evidence
  • ✓Permitted use stated per asset
  • ✓Affiliate adaptation guidance

Where no scientific platform exists, we will tell you, because otherwise the deck becomes the platform without anyone deciding that it should.

Deliverables Request a quote
Training

MSL training

For new teams or new data

Quoted per projectBased on team size and format

Delivery Agreed at scoping

  • ✓Scientific training on the evidence
  • ✓Scenario training on unscripted questions
  • ✓Boundary worked through by example
  • ✓Escalation routes practised
  • ✓Assessment and refresher materials

Scenario practice is what MSLs apply in real conversations. A walkthrough of the deck is not training.

Deliverables Request a quote
Insight capture

Insight system

For making field intelligence usable

Quoted per projectBased on team size and reporting need

Delivery Agreed at scoping

  • ✓Capture structure designed
  • ✓Taxonomy for themes and questions
  • ✓Reporting format for medical leadership
  • ✓Route into the medical and publication plans
  • ✓Training on what a usable insight looks like

Most insight programmes collect sentiment. The useful unit is a specific question from a specific setting, with a decision behind it.

Deliverables Request a quote

Send your current field deck and we will trace every claim to a source at no cost. Claims that originate in a field deck are the ones to identify.

FAQs

Frequently Asked Questions About MSL and Field Medical Materials

If your question is not answered here, please ask an expert. No quote is required.

The practical markers are who raised the topic, whether the content is balanced, whether it stays within what the evidence supports, and whether the interaction is documented as scientific.

The boundary is easier to teach through worked examples than through principles, so our training uses scenarios rather than definitions.

MSLs may respond to an unsolicited question within a defined process, with the response provided by medical information rather than improvised during the conversation.

Raising off-label use proactively is not scientific exchange. The framework depends on the distinction between responding and raising.

Follow your own SOP. Many organisations route field medical materials through medical review rather than full MLR, because they are non-promotional.

Whichever route you use should be documented and consistent, because an inconsistent review history is itself a finding.

This usually happens because the deck was built as a presentation rather than as a resource for a conversation that the clinician directs.

The solution is a short core narrative supported by detailed reference material and reactive sets, with training on moving between them, rather than a longer deck.

Related Services

Related Medical Affairs Services

Field medical work applies the scientific platform in real conversations with clinicians.

Request a Free Claim Traceability Check of Your Field Deck

It is better to identify a claim that first appears in a field deck, rather than in the platform, before anyone else finds it.

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Regulations

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Material you send is held under signed confidentiality, with access limited to the assigned team and encrypted transfer. It is not used to train anything and is not passed to third-party tools. Ask for the agreement before you send anything you would rather cover first.