We are excited to announce that Remco Munnik, our Regulatory Information Director, will be speaking on Wednesday, Feb 13 at 8.30 a.m., in the DIA’s Regulatory Submissions, Information, and Document Management (RSIDM) Forum (USA), about “Preparing Regulatory Affairs for the use of SPOR/IDMP and the benefits it can bring.”
Remco has over fifteen years’ experience in European and FDA submission procedures and is a specialist in electronic submission and regulatory data management. His team is composed of experts in eCTD global level, xEVMPD compliance and IDMP implementation.
DIA’s Regulatory Submissions, Information, and Document Management (RSIDM) Forum provides the elements needed to meet the challenges of optimizing the efficient use of regulatory information: the RIM principles, effective processes and tools, benefits to data applications across the product lifecycle, and examination of real-life results.
This event also provides multiple opportunities for networking, knowledge sharing, and education for both business- and technology-focused attendees.
