Author: ddregpharma

The INVIMA is the regulatory agency of Colombia that was established in 1992. It implements guidelines and standards to why Regulatory Services in Colombia must adhere to for product approval... Read More

The SAHPRA is in charge of all safety activities and Regulatory Services in South Africa, such as registering, monitoring, exploring, evaluating, and inspecting pharmaceutical products to ensure timely access to... Read More

The PMDA provides scientific analyses of pharmaceutical and medical device marketing applications, post-marketing safety monitoring and guidelines for Regulatory Services in Japan. This ensures MAHs can get their products to... Read More

In ASEAN countries, the Philippines ranks third in terms of pharmaceutical market size, behind Thailand and Indonesia. Our regulatory services in the Philippines can assist foreign manufacturers in successfully navigating... Read More

The pharmaceutical market of Egypt is one of the largest in the Middle East and North Africa (MENA) region. The Egyptian Drug Authority (EDA), which operates under the supervision of... Read More

Regulatory services in Kenya follow guidelines and requirements set by the Pharmacy and Poisons Board (PPB) which is the Drug Regulatory Authority established under the Pharmacy and Poisons Act. It... Read More

The goal of our regulatory services in South Africa is to empower the foreign manufacturer with the knowledge and understanding of the regulatory and compliance environment related to their pharmaceutical... Read More

Regulatory services in Kenya follow guidelines and requirements set by the Pharmacy and Poisons Board (PPB) which is the Drug Regulatory Authority established under the Pharmacy and Poisons Act. It... Read More

Our regulatory services in UK assists foreign manufacturers with localized Regulatory Affairs and operational support for required Regulatory procedures and stay ahead of any compliance risks. For more information, contact... Read More