Good Distribution Practice (GDP) Seminar for Pharma

Gstudy > Courses and seminars > Good Distribution Practice (GDP) Seminar for Pharma

By Iris Shamir, M.Sc.

3.0

Quality Assurance

Audits

Location: Online

Starts at: 09:30

Duration: Half day Seminar

Language: Hebrew

The GDP (Good Distribution Practice) course provides participants with a comprehensive overview and practical tools for implementing proper distribution principles for pharmaceuticals, in full alignment with international regulatory requirements and authority expectations.

Throughout the training, participants will gain knowledge and hands-on insights on key topics, including:

  • Regulations, Standards and Guidelines – understanding the global regulatory framework

  • Key Definitions – establishing a common professional language across all stakeholders

  • Serialization – preventing counterfeiting and enhancing supply chain traceability

  • Shipping Qualifications – ensuring validated shipping methods and product integrity during transportation

  • Temperature Management – applying best practices to maintain product quality during distribution

  • Challenges in Distribution Lanes – identifying risks and developing effective mitigation strategies

  • Authority Observations – learning from regulatory inspections and audits to improve readiness and compliance

 

This course combines theoretical knowledge with practical case studies, enabling participants to leave with a solid understanding and immediately applicable tools for their daily operations.

Who should attend?
Importers, distributors, logistics managers, and staff working in trading companies and distribution centers who wish to strengthen their expertise in GDP compliance and operational excellence.

Date and hours:   09:30-12:00 On-Line    
  • About Iris Shamir, M.Sc.

    Former GMP inspector at the Pharmaceutical Inspection Division of the Israeli Ministry of Health’s Institute for Standardization and Control (ISCP). She served as a lead inspector in audits of laboratories, active pharmaceutical ingredient (API) manufacturers, dry production, semi-solid and liquid dosage forms, as well as wholesalers and importers.Iris participated as an inspector in audits of aseptic and sterile processes, biotechnological...

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