PIC/S scheduled its 2026 seminar for November 4-6 in Istanbul. The three-day event focuses on digital transformation in GMP. It follows the PIC/S Committee meeting hosted by Türkiye’s authority. The seminar supports international inspector learning and regulatory convergence. The result may influence how inspectors assess digital manufacturing systems.
How Do GMP, PIC/S, and training workshop Change Work?
Rapid digitalisation creates inconsistent knowledge about data, automation, AI, and system oversight across inspections. PIC/S is hosting a three-day international seminar focused on digital transformation in GMP. The seminar runs for three days, from November 4 through November 6, 2026.
Impact Across GMP, PIC/S, and training workshop
Positive effect: Shared inspector training can support more consistent risk-based assessments across participating authorities. Risk: Industry professionals cannot assume attendance alone predicts every future inspection expectation. Implementation challenge: Companies must interpret public outcomes and strengthen controls without reacting to unconfirmed conclusions.
Career Skills for GMP, PIC/S, and training workshop
The update matters because it changes how organisations plan, document, communicate, or control regulated work. Professionals do not need to predict every outcome. They should understand the verified change, identify role impacts, and build evidence around the most relevant skills.
Inside QC: Practical Career Impact
QC teams should review instrument software, audit trails, and electronic data flows. Candidates should connect this impact with evidence from projects, training, placements, or regulated workplace responsibilities.
- Daily-work impact: QC teams should review instrument software, audit trails, and electronic data flows.
- Learn or review: audit-trail review, laboratory-system control, and ALCOA+.
Next Results After 3 days
QA and technical teams should monitor published materials and compare them with current digital-system controls. Professionals should monitor the official source, assess documented gaps, and prepare role-specific examples before interviews, audits, submissions, or implementation work.
Build context with Computer System Validation in Pharma Guide and strengthen practical knowledge through Introduction to Computer Systems Validation.