Corporate Courses · Technical Language

[ Healthcare and Pharma – Corporate Courses ]

Communicate with confidence in a regulated environment. Technical language for healthcare and pharma teams: clinical trials, regulatory affairs, medical writing and conference communication – with realistic simulations from your day-to-day work. Practical, company-specific and measurable.

At a glance

Key facts about the training

[ 01 ]

Target groups

Clinical operations, regulatory, medical affairs, pharmacovigilance, quality, market access and communications.

[ 02 ]

Languages and levels

English (focus) and German for international professionals · A2–C2.

[ 03 ]

Formats and duration

1:1, small group (3–8), team · 60/90 min · intensive workshops and programmes.

[ 04 ]

Delivery

Online (MS Teams), on-site at your premises or at Eloquia (Frankfurt) · hybrid possible.

[ 05 ]

Organisation

Materials included · flexible scheduling · cancellation up to 24 h beforehand free of charge.

[ 06 ]

Quality

ISO 9001-based QM · data protection with external DPO · diversity and inclusion.

Benefits and outcomes

What your team gains

We train exactly the language that really matters in trials, regulatory contacts and conferences – precise, clear and correct. This is about supportive language skills; we make no approval or efficacy promises.

  • Confident communication with authorities, KOLs and international partners
  • Accurate written language for protocols, reports and medical writing
  • Confident terminology for clinical trials, regulatory, pharmacovigilance and GxP
  • Realistic simulations with study documents and regulatory dialogues
  • Direct, measurable feedback on language, clarity and impact
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Simulations and practice

  • Authority meeting EMA/FDA terminology, answer questions confidently
  • Investigator conversation explain protocol, clarify queries
  • Safety review communicate signals and measures precisely
  • Conference and poster present data, lead discussion
Content and modules

Examples from the curriculum

Clinical trials and protocols

Study design, protocols, endpoints; describe procedures and results clearly.

Regulatory affairs

EMA/FDA terminology, submissions, briefing documents and regulatory dialogues.

Pharmacovigilance and safety

Signals, adverse events, risk management; safety language precise and correct.

Medical writing

Reports, abstracts, publications; write clearly, in a structured and traceable way.

Conference and poster presentations

Present data, explain posters and lead scientific discussions.

Market access and HEOR

Communicate value dossiers, evidence and health economics persuasively.

Quality and GxP communication

SOPs, deviations, CAPA; GxP-compliant language in reviews and evidence.

Stakeholder conversations

KOLs, authorities and partners; clarify expectations and maintain relationships.

Simulations and practice

Train on real scenarios

We practise the situations that really occur in your team – so your language holds up under pressure.

  • Authority meeting with Q&A training
  • Investigator and site conversation
  • Safety and signal review
  • Medical writing workshop with live feedback
  • Conference talk and poster discussion
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Common occasions

  • International trials multinational teams and sites
  • Submissions and audits confidence in reviews and inspections
  • Publications abstracts and manuscripts in English
  • Onboarding get new professionals language-ready quickly
Course formats

Three routes to your goal

[ 01 ]

1:1 coaching

Individual goals, confidential content, flexible times.

[ 02 ]

Team training

Consistent terminology and processes across the whole team.

[ 03 ]

Intensive workshop

Condensed into 1–2 days, focused on concrete deliverables.

1NeedsTarget picture, use cases, sensitive content, framework conditions.
2PlacementLanguage level, terminology, priorities, measurement points.
3QuoteFormat, trainer profile, materials, schedule.
4Start and trackingRegular feedback, goal review, adjustments.
FAQ

Frequently asked questions

How large are the groups?

We recommend 3–8 people per level and use case. Alternatively as one-to-one tuition.

Can company-specific content be integrated?

Yes. Your own SOPs, protocol templates, terminology and real scenarios are incorporated.

Which online platform do you use?

MS Teams as standard; other tools on request.

What are the cancellation terms?

Appointments can be cancelled free of charge up to 24 hours beforehand.

Complementary skill sprints

Build up individual skills in a targeted way

Alongside tailored in-company training, our four-week Business English sprints build up individual skills in a focused way – bookable individually or for the team. A good fit for this area:

All in-company courses

Ready for the next step?

Clarify goals, level and time slots – then start. We will prepare a no-obligation quote for you.
+49 (0)69 23 00 20 · info@eloquia.com

Request a quote

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Christopher Mann
Your contact

Christopher Mann

Managing Director

cmann@eloquia.com · +49 (0)69 23 00 20