Capacity limited to the size of the room.
15th April
Assi (Workshop Room 1) 10:00 to 12:00
Qualification of laboratory equipment according to USP 1058 and data integrity
Telstar (Workshop room 2) 10:00 to 12:00
Commissioning and Qualification: From Traditional Approach to Verification Approach (ASTM E 2500) / Pharma 4.0. IOT data platform for predictive maintenance

Oqotech (Workshop room 1) 12:00 to 14:00
Validation of Computerized Systems for pharmaceutical laboratories according to GLP and GAMP 5

QTI (Workshop room 2) 12:00 to 14:00
Steam in the pharmaceutical industry Are you prepared for the new requirements in terms of pharmaceutical steam?
TDV (Workshop room 1) 15:30 to 17:30
Digital Quality, How the digital transformation affects the pharmaceutical quality system
AZIERTA (Workshop room 2) 15:30 to 17:30
Practical approach to the new regulation on medical devices: Critical aspects and resolution of real cases
16th April
Quality By Design (Workshop Room 1) 10:00 to 12:00
Risk Management 4.0. Practical examples for digitizing acquired knowledge
Audinnova (Workshop room 2) 10:00 to 12:00
Observations on inspections. Are we going to tell lies?
Azierta (Workshop room 1) 12:00 to 14:00
Nitrosamines: past, present and future
Qualipharma (Workshop room 2) 12:00 to 14:00
Don’t limit your possibilities in the market: Why not medicines, health products, nutritional supplements, cosmetics,…?
Asphalion (Workshop room 1) 15:30 to 17:30
Review and support of statements under MDR
BEC (Workshop room 2) 15:30 to 17:30
Are they cosmetics or OTC medicines for the US market? – Regulatory implications
Diversey (ALKEMI Room) 15:30 to 17:30
BPR new European regulation on biocides. Considerations for cleaning and disinfection of clean rooms and CIP processes in the pharmaceutical and cosmetic industry