EC Report
1.
Project Details
Whether it is a violation case and application is being submitted under Notification No. S.O.804(E) dated 14.03.2017 ? :
No
1.
Project Details
i. Proposal No. :
IA/UK/IND2/61486/2017
ii. MoEFCC File No. :
IA-J-11011/4/2017-IA-II(I)
iii.Short narrative of the project:
Ish Medicos Pvt Ltd
iv. Project Sector :
Industrial Projects-2
v. Company/Proponent :
ISH MEDICOS
vi.Details of State of the project
Details of State of the project
S.no.
State Name
District Name
Tehsil Name
1.
Uttarakhand
Dehradun
Vikasnagar
vii.Date of TOR Granted
29 Apr 2017
viii.TOR letter issued by Ministry:
Annexure-TOR letter
ix.Date of Submission for EC:
04 Jul 2017
x.Project Type:
New
2.
Uploaded Documents of EIA/EMP,Risk Assessment,Public Hearing etc.
i.EIA/EMP:
Annexure-EIA/EMP
ii.Risk Assessment:
Annexure-Risk Assessment
iii.Public Hearing:
Annexure-Public Hearing
iv. Date of Public Hearing:
30 Jun 2017
v. Uploaded Additional Report/Study/Document as desired by Ministry/EAC:
Annexure-Additional Report/Study/Document
vi. Uploaded Cover Letter:
Annexure-Cover Letter
vii.Remarks:
Public hearing exempted by EIC committee.
3.
Additional Detail Sought
Additional Detail Sought
Sno.
ADS Letter
Remarks
Date of ADS
1.
NA
The EAC, after detailed deliberations on the proposal, observed that the Principal EIA Notification, 2006 and the subsequent amendments therein, do not provide for the requirement of prior EC for drug formulation units. However, at the same time, as per the Ministry’s Notification dated 4th July, 2005, the proposals covered under the orange category are to be dealt with as industries requiring EC as per the Environment Impact Assessment Notification, 1994 issued vide No.S.O.60€ dated the 27th January, 1994. As such, there seems to be a contradiction and needs to be resolved by the Ministry. The Committee further desired that the matter may be examined in the perspective of present categorization of industries vis-à-vis the extant provisions of the EIA Notification, 2006 and the amendments
04 Sep 2017
2.
ADS Letter
Dear Sir, We would like to bring to your kind notice that application for obtaining the environment clearance for the above mention project was submitted to MoEF, New Delhi in December 2016. The first technical presentation (for TOR approval) was held before EAC meeting during Janaury 23, 2017 to January 25, 2017 and subsequently, TOR approval was granted on April 29, 2017. The aforesaid proposal was considered by the expert appraisal committee (Industry -2) EAC in its Meeting held from 28/08/2017 to 29/08/2017. The EAC, after detailed deliberations on the proposal, observed that the Principal EIA Notification, 2006 and the subsequent amendments therein, do not provide for the requirement of prior EC for drug formulation units. However, at the same time, as per the Ministry’s Notification dated 4th July, 2005, the proposals covered under the orange category are to be dealt with as industries requiring EC as per the Environment Impact Assessment Notification, 1994
01 Nov 2017
4.
Accredited Consultant Details
i. Accreditation status :
Yes
ii. Accreditation No. :
MIE(I)CA
iii. Name of Consultant:
Ravi shankar juyal
iv. Address :
338/II, Vasant Vihar, Phase-2,Dehradun-248006
v. Mobile No.:
9897622722
vi. Landline No.:
01352721446
vii. Email Id:
ish@ishpharma.com
5.
Undertaking
I hereby give undertaking that the data and information given in the application and enclosures are true to be best of my knowledge and belief and I am aware that if any part of the data and information found to be false or misleading at at any stage, the project will be rejected and clearance given, if any to the project will be revoked at our risk and cost.
i. Name of Applicant :
Ish
ii. Designation :
Director
iii. Name of Company(Applicant Name should not be given here) :
ISH MEDICOS
iv. Address :
15, Kanawali road, Dehradun
v. Uploaded copy of documents in support of the competence/authority of the person making this application to make application on behalf of the User Agency:
Annexure-Uploaded copy of documents in support of the competence/authority of the person making this application to make application on behalf of the User Agency
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