Sliders – LAR PH

A LAR is responsible for handling post-market surveillance, adverse event reporting, and product recalls, providing a local point of contact for regulatory authorities, which is crucial for ongoing market access.

With the local knowledge and established relationships with regulators, a LAR can expedite the approval process, allowing faster entry into the Philippines market and enabling companies to start selling their medical devices sooner.

LARs keep companies informed about the latest regulatory updates and policy changes in the Philippines , ensuring ongoing compliance and helping to adapt strategies quickly when needed.

LARs act as a direct communication link between the company and Philippines regulatory bodies, effectively addressing any questions, requests for additional information, or changes in requirements.

A LAR ensures that all requirements set by FDA are met, helping companies stay compliant with current regulations and avoid penalties or product recalls.

A LAR has the local expertise and understanding of regulatory procedures, helping to navigate complex documentation and submission requirements. This streamlines the registration process, reducing the risk of delays and rejections.