For every country, the health of its people is of utmost importance. To maintain the
health of the people country has to ensure the quality of medicines and other
pharmaceutical products as well as devices. So, every country has its regulatory
authority which regulates the following:
1. Import of drugs from another country
2. Export of drugs to another country
3. Manufacturing of drugs in the country
4. Establishment of manufacturing companies in the country
7. Approval for clinical trials
8. Testing of drugs in the certified laboratories
9. The compliance with international guidelines
11. Issuing various types of licence related to drugs
ROLE OF REGULATORY AFFAIRS DEPARTMENT
Drug regulatory affairs is a dynamic and challenging field in the pharmaceutical
industry. It has to deal with government authority on one hand and applicant/company
on another hand. Because of the crucial nature of the job regulatory affairs professionals
should be experts in managing the product life cycle. They should have the capability
to solve technical as well as administrative problems within the limits of laws and
regulations. Regulatory affairs department is a bridge between government regulatory
authority and pharmaceutical company. It also has a connection with all the
departments of the company internally.
Regulatory affairs department plays many important roles. These are as follows:
• Keep other departments updated
• Helps in the execution of clinical plan
RESPONSIBILITY OF REGULATORY AFFAIRS PROFESSIONALS
There are some qualities which make efficient regulatory professionals. These are:
Because of the critical nature of this job, there are several important responsibilities
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