Skilful drafting of technical documentation
- 1° EDITION: 5 November 2024
- 2° EDITION: 15 April 2025
- Online
-
Italian
- 1° EDITION: 5 November 2024
- 2° EDITION: 15 April 2025
- Online
-
-
Italiano
-
Training overview
“If you cannot write well, you cannot think well; if you cannot think well, others will do your thinking for you” (Oscar Wilde). How much does effective writing influence the writing of technical documents? What are the crucial elements of being skilful in writing? How important is it to know how to communicate effectively with technical stakeholders such as institutions or a client? Writing to communicate is different from writing to inform. The lecturer during the training course “Skilful drafting of technical documentation” will illustrate both technical and communicative key aspects that are fundamental to producing effective and context-appropriate documents. Examples from the pharmaceutical world will help to understand the key concepts and how to put them into practice. The course will include a practical exercise to consolidate the principles explained.
Are you interested in Regulatory Affairs training?
Enroll in 3 courses and you’ll get a 15% discount*, while choosing 5 courses will grant you a 20% discount*!
Choose among these titles:
- CTD Modulo 3: I Punti Critici
- La Scrittura Efficace dei Documenti Tecnici
- Aspetti Regolatori degli Integratori Alimentari e Novel Food
- Focus sul Modulo 5 del CTD
- Requisiti Registrativi per gli APIs in area extra EU
- La Registrazione di un Farmaco: Linee-Guida di Tossicologia e Struttura CTD per la Sezione Preclinica
- Impatto Regolatorio dei Cambi
- Affari Regolatori: Le Basi dei Regulatory Affairs
- Building a Successful DMF Application Strategy for API, Excipient, and Packaging Material Registration in China – English training
- Marketing Authorization Holder (MAH), Affari Regolatori e Qualified Person: Responsabilità ed Interazioni per la Compliance GMP
- La Gestione delle Elemental Impurities
(*) discounts apply to the full prices of the courses and cannot be combined with other promotions.
The promotion is limited to enrolling the same person in 3 or 5 courses selected from those offered.
Key points of the training
- What it means to communicate and inform
- Effective written communication
- Writing appropriately to the context and the speaker
09:00 – 12:00 COURSE SESSION
- Written and oral communication
- Critical reading of a document and emotional aspects
- Thinking before writing
- Focus on key points for effective writing
- How to structure a document considering the cultural factors of the speaker (examples)
- Practical exercise
Professionals involved in the pharmaceutical sector: Regulatory Affairs, Quality Assurance, R&D, Quality Control.
The course will be carried out through live lectures. Practical examples will be showcased, providing delegates with real life examples to be applied in their daily job life.
For online trainings the access link will be sent 2-3 days before the start of the training.
5% discount for registrations within 1 month before the start of the training, 10% discount for registrations within 2 months before the start of the training. VAT not included. Please inquire for discounts for multiple registrations. Discounts are not cumulative.
Cancellation terms
In order to cancel enrolment to an event, please email info@pharmaeducationcenter.it within 2 weeks before the starting date of the event. Once this term will be expired, the entire fee will be charged.
Participant replacement
It is possible to replace a participant attendance without additional cost, simply by contacting info@pharmaeducationcenter.it. It is asked to notify the participant replacement request within 5 days before the starting date of the course/event, specifying the full name and surname of the enrolled participant as well as the full name and surname of the substitute.
Training cancellation
If the minimum number of participants is not reached, Pharma Education Center reserves the right to cancel or schedule the event for another date. Formal communication will be given within 5 days before the event date. In this case Pharma Education Center will refund the registration fee in full and without additional charges. Alternatively, the participant can request a spendable coupon for participating in another PEC event scheduled in the current year.
Speakers
Lorenza Moscarella
Llifescience consultant, business coach
She has thirteen years of professional experience in chemical-pharmaceutical companies with different production sites, types of products (finished products and/or active ingredients), types of markets and different Regulatory Authorities around the world. She has a strong background in Regulatory (FDA, ICH, EudraLex,) RDC (Brazilian API Regulatory) and other CMC requirements for different types of authorities around the world, as well as Quality Assurance regulations (GMP, ICH, EudraLex, Pharmacopoeia, ISPE). Inspection experience from AIFA, FDA, Swiss Medic.
Register now
450€
Training materials available for attendees
Certificate of attendance
Senior trainers with hands-on experience
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