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Details van artikel 18 van 18 gevonden artikelen
| Titel: |
Vaccine policy, regulations and safety in India |
| Auteur: |
Gogtay, N.J. Dhingra, M.S. Yadav, A. Chandwani, H. |
| Verschenen in: |
International journal of risk & safety in medicine |
| Paginering: | Jaargang 21 (2009) nr. 1-2 pagina's 23-30 |
| Jaar: |
2009-05-20 |
| Inhoud: |
Vaccine development in India, though slow to start, has progressed by leaps and bounds in the past 60 years transforming it from a nation completely dependent on imported vaccines to one not only self-sufficient in the production of vaccines conforming to international standards, but also a major supplier of the same to UNICEF. Vaccine development is tightly regulated by a hierarchy of regulatory bodies. Guidelines provided by the Indian Council of Medical Research (ICMR) set the rules of conduct for clinical trials from Phase I to IV studies as well as studies on combination vaccines. These guidelines address ethical issues that arise during a vaccine study. A network of Adverse Drug Reaction (ADR) monitoring centers along with the Adverse Events Following Immunization (AEFI) monitoring program provide the machinery for vaccine pharmacovigilance. |
| Uitgever: |
IOS Press |
| Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
Details van artikel 18 van 18 gevonden artikelen
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