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Pharmaceutical

Pharmaceutical

English for the pharmaceutical industry is specifically for people who need to communicate effectively in English in the pharmaceutical industry. This programme covers the full process of drug development from medical research and development, quality control and auditing to drug safety and trials, manufacturing and packaging. This programme will equip learners with the linguistic skills and vocabulary necessary to understand daily situations in a work environment.

10
Hours
Workshop

Cumartesi - Pazar
10:00 / 16:00

(2 Gün Toplam 10 Saat)
Workshop Çalışması

4 People 3.250 TL
8 People 2.000 TL
12 People 1.499 TL

24
Hours
Intensive

Ptesi - Çarş - Cuma
19:00 / 21:00

(4 Hafta Toplam 24 Saat)
Yoğun Program

4 People 7.999 TL
8 People 4.999 TL
12 People 3.999 TL

32
Hours
Complete

Salı - Perşembe
19:00 / 21:00

(8 Hafta Toplam 32 Saat)
Detaylı Eğitim

4 People 9.999 TL
8 People 5.999 TL
12 People 4.999 TL
KURUMSAL İNGİLİZCE EĞİTİMİ

Business English® training programmes are based on the training needs of your company. No matter what your sector, we can train your staff to become confident and functional users of English to communicate effectively at work.

İŞ İNGİLİZCESİ KURSLARI

As the global language of choice in business, many corporations expect their employees to communicate competently in English. At Business English®, you will learn how to express yourself more fluently and confidently at work.

İNGİLİZCE ÖZEL DERS

Business English® private English lessons are aimed at meeting your individual language learning needs. Your programme is flexible which enables progress in the language skills you need to develop to advance your career.

  • 1 THE KICK-OFF MEETING
    • 1.1 Job titles and responsibilities
    • 1.2 New drug development and launches
    • 1.3 Cultural differences in marketing drugs and medicine
    • 1.4 Providing information
    • 1.5 Introducing yourself, your field and projects
    • 1.6 Summarising action points
    • 1.7 Writing job ads
  • 2 SUBSTANCE DISCOVERY AND PRODUCT DEVELOPMENT
    • 2.1 A new chemical entity (NCE)
    • 2.2 Drug dosage forms
    • 2.3 Categories of drugs
    • 2.4 Asking about drug discovery and drug development
    • 2.5 Talking about time periods
    • 2.6 Asking for and giving opinions
  • 3 QUALITY ASSURANCE AND AUDITING
    • 3.1 Good pharmaceutical industry practice (GxP)
    • 3.2 Quality assurance audits
    • 3.3 Laboratory safety systems
    • 3.4 Standard operating procedures
    • 3.5 Informing
    • 3.6 Asking questions during an audit
    • 3.7 Suggesting corrective action
    • 3.8 Discussing SOPs
  • 4 READY FOR TESTING IN LIVE ORGANISMS
    • 4.1 Preclinical testing
    • 4.2 Clinical testing
    • 4.3 Dealing with authorities
    • 4.4 Experimental drugs on trial
    • 4.5 Describing a process
    • 4.6 Getting information
    • 4.7 Making suggestions
    • 4.8 Linking ideas
    • 4.9 Requesting information and responding directly
  • 5 DRUG SAFETY AND REGULATORY AFFAIRS
    • 5.1 Pharmacovigilance
    • 5.2 Regulatory documentation
    • 5.3 Patient information
    • 5.4 Counterfeit medicines
    • 5.5 Reporting severe adverse events
    • 5.6 Discussing the causes of SAEs
    • 5.7 Asking about implications for a drug
    • 5.8 Giving general advice
    • 5.9 Giving strong warnings
  • 6 PRODUCTION AND PACKAGING
    • 6.1 Safety requirements
    • 6.2 Production processes
    • 6.3 Packaging challenges
    • 6.4 Expressing moments in time
    • 6.5 Giving instructions
    • 6.6 Describing a process
    • 6.7 Giving presentations