Post by Normec Advipro

Did you know that...due to the update of Eudralex Volume 4 Annex 11, your organization will need to perform a GAP analysis on current processes and systems? Procedures, contracts, and SLAs must be reviewed. Staff in QA, IT, and operations roles must be also trained in the new requirements. QA and compliance teams are responsible for validation, audits, and ensuring quality. With increasing focus on computerized systems, data integrity, and compliance, staying aligned with Annex 11 is more critical than ever for pharma and life sciences companies. But… are your systems and processes fully compliant? That’s where we can help. 𝗔𝘁 𝗡𝗼𝗿𝗺𝗲𝗰 𝗔𝗱𝘃𝗶𝗽𝗿𝗼, 𝘄𝗲 𝘀𝘂𝗽𝗽𝗼𝗿𝘁 𝗼𝗿𝗴𝗮𝗻𝗶𝘇𝗮𝘁𝗶𝗼𝗻𝘀 𝗶𝗻 𝗶𝗱𝗲𝗻𝘁𝗶𝗳𝘆𝗶𝗻𝗴 𝗴𝗮𝗽𝘀 𝗮𝗻𝗱 𝘁𝗿𝗮𝗻𝘀𝗹𝗮𝘁𝗶𝗻𝗴 𝗿𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗿𝗲𝗾𝘂𝗶𝗿𝗲𝗺𝗲𝗻𝘁𝘀 𝗶𝗻𝘁𝗼 𝗽𝗿𝗮𝗰𝘁𝗶𝗰𝗮𝗹 𝗮𝗰𝘁𝗶𝗼𝗻𝘀. 𝗢𝘂𝗿 𝗦𝗲𝗻𝗶𝗼𝗿 𝗖𝗼𝗻𝘀𝘂𝗹𝘁𝗮𝗻𝘁𝘀 𝗮𝗻𝗱 𝗚𝗠𝗣 𝘀𝗽𝗲𝗰𝗶𝗮𝗹𝗶𝘀𝘁𝘀 𝗮𝗿𝗲 𝗮𝘃𝗮𝗶𝗹𝗮𝗯𝗹𝗲 𝘁𝗼 𝗴𝘂𝗶𝗱𝗲 𝘆𝗼𝘂 𝗲𝘃𝗲𝗿𝘆 𝘀𝘁𝗲𝗽 𝗼𝗳 𝘁𝗵𝗲 𝘄𝗮𝘆. 👉 Curious to learn more? https://lnkd.in/e9Z3z4Qk