Regulation and compliance · News
Zonal Offices of CDSCO May Be Grated Powers For Issuing Licences Under CDA
The Centre may tone down the much-criticised provision of issuing manufacturing licences only by a cetralised agency based in Delhi under the proposed Central Drug Authority of India, by empowering the zonal offices o…
The Centre may tone down the much-criticised provision of issuing manufacturing licences only by a cetralised agency based in Delhi under the proposed Central Drug Authority of India, by empowering the zonal offices of the Central Drugs Standard Control Organization (CDSCO) also to issue licences.
The Parliamentary standing committee on health on family welfare, which has been examining the Drug and Cosmetics (Amendment) Bill 2007 seeking to set up the CDA, is likely to make a recommendation in this regard. The Committee has recommended that instead of entrusting entire powers of the State licensing authorities with the CDA, four zonal offices of the CDSCO should also be made licensing authorities for the respective regions, it is learnt.
The clause in the bill to centralise the licensing system had invited srath from different quarters especially the small and medium scale companies and associations representing them during the sitting of the parliamentary panel headed by Amar Singh. The small scale drug manufacturers accused the proposed CDA as a ‘tool’ to make their lives worse. It would be nearly impossible for the manufacturers based in different corners of the country to come and seek licences from Delhi for every drug, they claimed.
Taking into consideration theses difficulties, the Parliamentary committee is understood to have made the suggestion for devolution of the powers to the zonal offices, so that the original goals of having a centralised regime for streamlining and monitoring the sector could still be met even while ensuring better logistics for the industry. As zonal wings are directly manned by the Central office, the entire licensing system still remain centralised. This would also lead to procedural delays which could happen due to piling up of applications at one point.
(Ref : Chronicle Pharmabiz dated October 2, 2008)