Regulatory-related tasks (such as responding to approval applications)
We provide consistent support from the formulation of regulatory response strategies for pharmaceuticals to the preparation, review, and submission of necessary documents!
When a company expands overseas, it is necessary to be well-versed in the local laws to comply with local regulatory requirements and avoid regulatory violations and delays in approvals. Experienced regulatory compliance consultants with practical experience in the pharmaceutical and medical device industries provide support services tailored to your needs, ensuring that related documents comply with stringent regulations. [Pharmaceutical Sector] We support product registration in the EU, China, the United States, and Latin America, monitor and track progress, and communicate with regulatory authorities on behalf of our clients. [Medical Device Sector] We prepare registration documents and technical materials for MD and IVD products.
- Company：PQE Japan
- Price：Other
