“𝘐𝘵 𝘪𝘴 𝘨𝘳𝘦𝘢𝘵 𝘵𝘰 𝘴𝘦𝘦 𝘺𝘰𝘶 𝘵𝘢𝘭𝘬 𝘢𝘣𝘰𝘶𝘵 𝘰𝘶𝘳 𝘤𝘶𝘳𝘳𝘦𝘯𝘵 𝘤𝘩𝘢𝘭𝘭𝘦𝘯𝘨𝘦𝘴, 𝘢𝘯𝘥 𝘩𝘰𝘸 𝘸𝘦 𝘤𝘢𝘯 𝘪𝘮𝘱𝘳𝘰𝘷𝘦 𝘸𝘩𝘢𝘵 𝘸𝘦 𝘥𝘰 𝘵𝘰𝘥𝘢𝘺. 𝘞𝘩𝘪𝘭𝘦 𝘢𝘭𝘭 𝘵𝘩𝘦 𝘵𝘢𝘭𝘬 𝘢𝘣𝘰𝘶𝘵 𝘥𝘢𝘵𝘢 𝘪𝘴 𝘨𝘳𝘦𝘢𝘵, 𝘸𝘦 𝘴𝘵𝘪𝘭𝘭 𝘩𝘢𝘷𝘦 𝘵𝘰 𝘶𝘴𝘦 𝘥𝘰𝘤𝘶𝘮𝘦𝘯𝘵𝘴 𝘧𝘰𝘳 𝘢𝘭𝘮𝘰𝘴𝘵 𝘦𝘷𝘦𝘳𝘺𝘵𝘩𝘪𝘯𝘨 𝘸𝘦 𝘥𝘰 𝘵𝘰𝘥𝘢𝘺.“ That's the feedback my colleague Geert Van Peteghem received after his presentation at the GPRAS conference last month in Brussels. Our upcoming webinar is going to focus on solving the challenges you face today: 𝐇𝐨𝐰 𝐝𝐨 𝐲𝐨𝐮 𝐦𝐚𝐤𝐞 𝐬𝐮𝐫𝐞 𝐲𝐨𝐮 𝐬𝐩𝐞𝐧𝐝 𝐚𝐬 𝐥𝐢𝐭𝐭𝐥𝐞 𝐭𝐢𝐦𝐞 𝐚𝐬 𝐩𝐨𝐬𝐬𝐢𝐛𝐥𝐞 𝐰𝐡𝐞𝐧 𝐩𝐫𝐞𝐩𝐚𝐫𝐢𝐧𝐠 𝐜𝐨𝐫𝐫𝐞𝐜𝐭𝐥𝐲-𝐟𝐨𝐫𝐦𝐚𝐭𝐭𝐞𝐝, 𝐜𝐨𝐦𝐩𝐥𝐢𝐚𝐧𝐭 𝐏𝐃𝐅𝐬 𝐟𝐨𝐫 𝐠𝐥𝐨𝐛𝐚𝐥 𝐬𝐮𝐛𝐦𝐢𝐬𝐬𝐢𝐨𝐧𝐬? You will find the answer in one of our sessions on December 14. The link to both sessions is in the comments. See you there! #regulatoryoperations #pharmaceuticals #regulatorysubmissions #PDF #automation