Regulatory Intelligence & PV Expertise in AFRICA

Regulatory Intelligence & PV Expertise in AFRICA Our Pharmacovigilance (PV) Team in Africa brings a wealth of expertise in Regulatory Intelligence and Pharmacovigilance processes. With a deep understanding of both post-commercialized products and clinical trial legislation, our team is well-equipped to navigate the intricate regulatory landscapes across various countries in the African region. The varied […]

PV Expertise in MEXICO

PV Expertise in MEXICO Mandatory XML SubmissionAs part of the regulatory updates, it is important to note that the submission of adverse event reports in the XML (E2B) format will become mandatory for all pharmaceutical companies in Mexico. This shift underscores the need for companies to prepare for compliance with the new requirements. The implementation […]