Find out how and why it becomes crucial for companies to have it to address the regulatory requirements, obtain the market entry, and ensure the product quality for its successful sales in the highly promising Japanese market.Read More

Clarify its key role in ensuring regulatory compliance and patient safety, by examining its components, submission process and implications for pharmaceutical companies and regulatory authorities.Read More

Aceclofenac is a prescribed medicinal product for pain relief and inflammatory conditions. Being a nonsteroidal anti-inflammatory drug (NSAID).Read More

The Drug Master File is a confidential document submitted to the regulatory authorities by pharmaceutical manufacturers. Detailed information on the production process, quality control and safety of an active pharmaceutical ingredient API is included.Read More

A Drug Master File (DMF) is a complex confidential document submitted to the regulatory authorities, which contains detailed info on pharmaceutical products.Read More