Academy
Explore Open Courses
Learn. Grow. Lead Healthcare Forward
GSAP Academy transforms decades of hands-on experience into practical, expert-led training for life sciences professionals. Our programs help individuals and organizations build capabilities, stay current with industry requirements, and apply knowledge immediately in the workplace.
Learn from Experts Who Lead Real-World Projects
Every program is developed and delivered by experts actively leading regulatory, quality, engineering, validation, and clinical projects across the life sciences and healthcare sectors. Our programs combine current regulations, real-world case studies, lessons learned, and proven methodologies, providing actionable insights that go beyond theory and are drawn from current industry challenges.
Designed for Every Career Stage
Whether you are entering the industry, expanding your expertise, preparing for a new role, or maintaining professional qualifications, GSAP Academy offers relevant training tailored to your needs. Our programs support individual professional development while enabling organizations to strengthen internal expertise and capabilities.
Training Programs
Programs are delivered in classroom-based and live virtual formats, providing an interactive and practical learning experience tailored to specific training objectives and audience needs
Professional Courses & Seminar Days
Designed to build professional knowledge and expertise, strengthen understanding of current regulatory requirements, and provide practical tools for implementation within organizations
Lead Auditor Training Courses
Tailored specifically for professionals in the medical device and pharmaceutical sectors. Gain the expertise you need to conduct thorough audits and drive compliance within your organization
Customized In-House Training Programs
Tailored to an organization's specific needs, work processes, and regulatory requirements, including annual training, courses, workshops, and seminars
Courses & Seminar Days
Medical Device ISO 13485 Quality Management System Requirements Training – The course is fully booked
By Dana Manaim-Tirosh
ISO 13485:2016 Quality Management Systems Course The course is fully booked This comprehensive course provides in-depth knowledge and practical skills for implementing and maintaining ISO 13485:2016 Quality Management Systems in…
Medical Device Quality and Regulation Training Course – Full
By Sivan Luder & Dana Manaim-Tirosh & Avital Levertov
Medical Device Quality and Regulation Course Registration for the first two seminar days is now closed Registration is still open for the remaining three days This comprehensive course provides in-depth…
Auditor Certification Course for the Pharmaceutical Industry A practical, pharma-focused course for professionals who plan, conduct, document and follow up on internal, external and supplier audits. The course provides practical…
Validation Engineers Qualification Course for Systems and Equipment – Pharmaceutical Industry
By Elias Morany
Validation Engineers Training Course for the Pharmaceutical Industry Join our specialized training course for Validation Engineers in the Pharmaceutical Industry, focusing on the validation life cycle for systems and equipment…
FDA Requirements: Quality & Regulatory Essentials for Medical Devices – 1-Day Seminar This seminar introduces key medical device regulations, the main FDA regulatory pathways for 510(k) clearance, De Novo granting…
Medical Device EU MDR Seminar – Regulation (EU) 2017/745
By Dana Manaim-Tirosh
Medical Device EU MDR 1-Day Seminar This comprehensive seminar provides essential knowledge for navigating the EU Medical Device Regulation (MDR) 2017/745 requirements. Designed for medical device professionals, the seminar focuses…
Verification and Validation (V&V) for Medical Devices A professional, practice-oriented course that provides a clear and solid foundation for understanding, planning and implementing Verification and Validation activities as an integral…
Cleaning Validation Seminar for the Pharmaceuticals Industry
By Iris Shamir
Cleaning Validation Seminar for the Pharmaceutical Industry The seminar reviews the regulatory requirements and guidelines throughout the cleaning validation lifecycle. Participants will learn from examples of regulatory authorities’ observations, explore…
Medical Device Risk Management Seminar (ISO 14971:2019)
By Sivan Luder
Medical Device Risk Management – ISO 14971:2019 and ISO/TR 24971:2020 This interactive training provides a comprehensive understanding of ISO 14971:2019 and ISO/TR 24971:2020 and the application of risk management principles…
Process Validation (PV) for Medical Device Industry
By Jose (Yossi) Chvaicer
Medical Device Risk Management – ISO 14971:2019 and ISO/TR 24971:2020 This interactive training provides a comprehensive understanding of ISO 14971:2019 and ISO/TR 24971:2020 and the application of risk management principles…
FDA QSR to QMSR Transition Training – Online
By Sivan Luder
QMSR Transition Training: Adapting to the New FDA Regulation The FDA’s new Quality Management System Regulation (QMSR) has officially replaced 21 CFR Part 820 and incorporates ISO 13485:2016 by reference.…
Everything That Matters in Medical Device EtO Sterilization Validation This practical two-day masterclass provides teams with the knowledge needed to understand, control and justify Ethylene Oxide (EtO) sterilization throughout the…
GMP Laboratory Analyst Qualification
By Rivka Goldik
GMP Laboratory Analyst Certification This practical two-day training course is designed to qualify analysts for proper and compliant work in Quality Control laboratories in the pharmaceutical and medical device industries.…
Medical Device Lead Auditor Certification Course
By Dana Manaim-Tirosh
Medical Device Lead Auditors Certification Course The objective of this course is to provide participants with the knowledge and practical skills required to perform first-party, second-party and third-party audits of…
Clean Rooms and HVAC Systems – Qualification, Validation and Monitoring (Medical Device & Pharma)
By Elias Morany & Meir Podriadchik Paz
HVAC Systems and Cleanrooms Professional Certification Course This intensive two-day program is designed for professionals in the pharmaceutical and medical device industries who work with HVAC systems and cleanrooms. The…
Computerized Software Validation (CSV)
By Sara Levy
Computerized Software Validation (CSV) Course This three-day course provides a comprehensive and structured overview of global regulatory requirements for Computerized Software Validation, including FDA 21 CFR Part 11, EU GMP…
Medical Device Quality and Regulation Training Course – Full
By Sivan Luder & Dana Manaim-Tirosh & Avital Levertov
Medical Device Quality and Regulation Course Registration for the first two seminar days is now closed Registration is still open for the remaining three days This comprehensive course provides in-depth…
Medical Device ISO 13485 Quality Management System Requirements Training
By Dana Manaim-Tirosh
ISO 13485:2016 Quality Management Systems Course The course is fully booked This comprehensive course provides in-depth knowledge and practical skills for implementing and maintaining ISO 13485:2016 Quality Management Systems in…
FDA Requirements: Quality & Regulatory Essentials for Medical Devices – 1-Day Seminar This seminar introduces key medical device regulations, the main FDA regulatory pathways for 510(k) clearance, De Novo granting…
Medical Device EU MDR Seminar – Regulation (EU) 2017/745
By Dana Manaim-Tirosh
Medical Device EU MDR 1-Day Seminar This comprehensive seminar provides essential knowledge for navigating the EU Medical Device Regulation (MDR) 2017/745 requirements. Designed for medical device professionals, the seminar focuses…
Medical Device Risk Management Seminar (ISO 14971:2019)
By Sivan Luder
Medical Device Risk Management – ISO 14971:2019 and ISO/TR 24971:2020 This interactive training provides a comprehensive understanding of ISO 14971:2019 and ISO/TR 24971:2020 and the application of risk management principles…
Validation and Verification of Analytical Methods – in Pharma & Medical Devices – Coming Soon
By Anat Sokol
Validation and Verification of Analytical Methods Professional Training Master the critical regulatory requirements and technical expertise essential for analytical method validation in pharmaceutical manufacturing. This comprehensive one-day seminar provides regulatory…
Pharmaceutical Quality Assurance Certification Course Quality on the Shop Floor in the Pharmaceutical Industry This course is designed for professionals looking to advance their careers through a practical, field-oriented role…
Out of Specification (OOS) Investigations: Advanced Training for Pharmaceutical QA – Coming Soon
By Jenny Sverdlova
Transform Your Out-of-Specification (OOS) Investigation Approach with Expert-Led Training This comprehensive seminar is designed to strengthen Out-of-Specification investigation capabilities through regulatory guidance, real-world inspection insights and advanced investigative methodologies. Participants…
Process Validation with focus on Quality Aspects for the pharmaceutical industry – On-demand
By Maya Gefen
Process Validation with Focus on Quality Aspects for the Pharmaceutical Industry – On-Demand This course offers an in-depth overview of process validation in the pharmaceutical industry, following FDA and EMA…
GDP (Good Distribution Practice) Course This course provides participants with a comprehensive overview and practical tools for implementing proper distribution principles for pharmaceuticals, in full alignment with international regulatory requirements…
Ready to Move Forward?
Whatever your next milestone is, let’s bring the right expertise together to get you there
Silvian Shama
Business Development Manager
Pharma & Advanced Therapies
Add. 2 Shaar Palmer St., Haifa, Israel