Training on Good distribution Practice (GDP)
- 1° EDITION: 21 October 2024
- 2° EDITION: 2 April 2025
- Online
-
Italian
- 1° EDITION: 21 October 2024
- 2° EDITION: 2 April 2025
- Online
-
-
Italiano
-
Training overview
This training course on Good Distribution Practice (GDP) will explain you the European and local regulatory environment for the distribution and marketing of medicinal products. The training will examine the application of the November 5 2013, Guidelines on Good Distribution Practice (GDP) of medicinal products for human use (2013/C 343/01), which establish the appropriate tools to assist wholesale distributors in carrying out their activities; these activities are carried out with manufacturers or their depositories.
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:
- Technology Transfer nel settore Farmaceutico – English training
- Ispezioni e Audit nel Farmaceutico
- Gestione dei risultati OOS e OOE/OOT
- Risk Analysis nel Farmaceutico
- Il Monitoraggio Ambientale nel Settore Farmaceutico
- Le Good Distribution Practices (GDP)
- La Convalida Analitica secondo ICH Q2
- Metodi Statistici per il Controllo Qualità
- APR, PQR e CAPA System
- Il Campionamento Ambito Farmaceutico
- Qualifica, Convalida di Processo e Cleaning Validation
- Inspection Readiness Documentale
- Investigational Medicinal Products: Aggiornamenti EU sugli IMPS
- La Convalida dei Metodi Microbiologici
- Studi di Stabilità nello Sviluppo Farmaceutico
- Ispezioni e Audit al Laboratorio QC Microbiologia
- RABS e Isolatori nella Produzione dei Farmaci Sterili
- Le Deviazioni Microbiologiche: Come Gestirle?
- Qualified Person: Giornate di Formazione
- Il Controllo Microbiologico nel Settore Farmaceutico
- Pharmaceutical Risk Assessment – English training
(*) 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
- Regulatory framework for product distribution and marketing
- GMP and GDP: general concepts
- Focus on Good Distribution Practice (GDP) of medicinal products
- Pharmaceutical transportation and safety aspects: measures to combat pharmaceutical crime
- Drug traceability
- The responsibility of the various actors in the drug supply chain
09:30 – 12:30 MORNING SESSION
14:00 – 17:00 AFTERNOON SESSION
- Regulatory framework and guidelines for medicinal products distribution and marketing
- GMP and GDP: general concepts
- The responsibility of the various actors in the drug supply chain
- Drug traceability
- Pharmaceutical transportation and safety aspects: measures to combat pharmaceutical crime
- Focus on Good Distribution Practice (GDP) of medicinal products:
- Quality Management
- Personnel and training
- Documentation
- Premises and Equipment and Operations: receipt and storage
- Complaints, returns, suspicions about falsified medicines, and medicine recalls
- Outsourced activities
- Self-inspections
- Broker
- Q&A time
Quality Assurance, Regulatory, Supply Chain and Logistics.
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
Paola Scavo
Process & Quality - Team Leader Senior Consultant at Pharma D&S
She graduated in Pharmaceutical Chemistry and Technology in Pisa, she has been working in Pharma D&S since 2014, where today she holds the role of Process & Quality Senior Consultant – Team Leader. She deals with the development of Quality Systems in the pharmaceutical and medical device fields and with Quality operational support for carrying out the maintenance activities of the Quality Systems for Marketing Authorization Holders/affiliates of multinationals, according to the applicable local legislation, the GMP/GDP/ GVP, the ISO 9001, ISO 13485 standards and the Farmindustria guidelines.
Register now
850€
Training materials available for attendees
Certificate of attendance
Senior trainers with hands-on experience
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