ARIES DRUGS PRIVATE LIMITED

Plot no. 90 Sector-IIDC, Sidcul, Pant Nagar- 263 145, UTTARAKHAND,

E-mail : ariesdrugslko@yahoo.com Website : www.ariesdrugs.com

SITE MASTER FILE

COMPANYS RESPONSIBLE PERSON
NAME MR. HARIOM AGARWAL MR. AMIT AGARWAL MR. ROBIN MATHEW Mrs. MUKUL AGARWAL Mr. SUSHANT RAI AGARWAL MR. ASHOK JAISWAL MR. KAILASH DASS MR. ANOOP DUTTA CHAIRMAN MANAGING DIRECTOR/ PLANT HEAD DIRECTOR DIRECTOR H.R & ADMINISTRATION. PRODUCTION IN-CHARGE QC IN-CHARGE STORE IN-CHARGE DESIGNATION

ARIES DRUGS PRIVATE LIMITED

CONTENTS
1.

GENERAL INFORMATION SPECIFIC INFORMATION PREMISES, FACILITIES AND EQUIPMENTS DOCUMENTATION PRODUCTION QUALITY CONTROL CONTRACT MANUFECTURER & LICENSEE DISTRIBUTION, COMPLAINTS, & PRODUCT RECALLS SELF- INSPECTION FLOW CHARTS - PRODUCTION DEPARTMENT: Material Movements & Oral Liquid Production FLOW CHARTS - QUALITY CONTROL DEPARTMENT: Sterility testing Packaging Material Analysis & Release In-process QA/QC & Finished Product Analysis Raw Material Analysis & Release LIST OF PRODUCTS SOP INDICES Quality Control Production Stores Administration Store Department Water System

2. 3. 4. 5. 6. 7. 8. 9. 10. 11.

12. 13.

14. 15. 16. 17.

PRODUCTION MACHINERY QUALITY CONTROL EQUIPMENTS ORGANIZATION CHART: Company Organ gram FLOW CHARTS: Engineering Store Management System Water System Preventive Maintenance Schedule MANPOWER STRENGTH

18.

1.0
1.1

GENERAL INFORMATION
Brief information of the Company
th

Aries drugs Pvt. Ltd. Was established in 2005 on the 4 day of April at LUCKNOW with five Directors. The company was established with 22 Medical representatives and five managers for its own marketing in Uttar Pradesh state. Aries started with the complete B2 range of products including Tablets, Capsules & Oral Liquids for its marketing; earlier the products were getting manufactured from Himachal & Haryana State under strict quality parameters. The vision of the company was to establish its own manufacturing unit within next four to five years. Therefore in this regard the company purchased the land for the manufacturing unit in Uttarakhand Integrated Industrial Estate at Pantnagar, Rudrapur. Aries now has established its own manufacturing unit specializing in Oral Liquid Plant only. This manufacturing facility has been designed with modern, automated processes, utilities and equipments conforming to national standards and cGMP norms amended from time to time. Facility has the capacity to produce complete Oral Liquid Unit. Using modern equipments, This manufacturing facility is national regulatory compliant and is futuristically designed. In our company has fully automatic equipments/Instruments for manufacturing. In all department supply fresh air & AHU with 0.5 filter. 1.2 Manufacture of pharmaceutical products The facility is dedicated for production of Antibiotics, Multivitamins, Cough Syrup, and Antialargic. All the above products are manufactured in the following dosage forms in Oral Liquid : Manufacturing License No. 17/UA/2009 IN FORM No. 25 and Manufacturing License No. 19/UA/SC/P-2009 in Form No. 28 are issued by Uttarakhand Drug Licensing Authority. 1.3 a) Our Contact details: Manufacturing Site: b) Head Office :

PLOT NO.90, SECTOR-IIDC, SIDCUL, PANTNAGAR-263145.(U.K)

E-mail : ariesdrugslko@yahoo.com Website : www.ariesdrugs.com Tel No : (05944) 250546, Mobile : 0 9335291146 / 0 9335291145

Aries Drugs Pvt. Ltd. S-89/16, D-Block, Rajajipuram,

Lucknow-226017.

Tel No. 0522-3298260

Mobile : 09335291145/46/47

1.4

Details of our Products and Process: PRODUCTION FLOW CHARTS RAW & PACKING MATERIAL MOVEMENT

RM/PM Receipt

De Dusting & Record

Recection. RM Return to party

Sampling, Testing

Rejection Report

Unprinted PM Return to party

Passes

Printed PM Destroy

Approved Material store

Dispensing

Primary PM

In-process

Sampling Testing

Passes

Rejection Report Rejected

Semi Finished Product

Rework

Destroy

Sampling Testing

Passes

Packaging

Finished Product

Quality Approved

Dispatch

1.5

REFER LIST OF PRODUCTS LIST OF PRODUCTS

Sr No 1. 2.

BRAND NAME POLYFER SYRUP ARIZYME SYRUP

COMPOSITION
Each 5 ml contain. IRON (III) HYDROXIDE POLYMALTOSE COMPLEX FOLIC ACID I.P. Each 5 ml contain.
FUNGAL DIASTASE(1:12000) I.P.

PACK
200 ML

50mg. 0.5mg

3.

FECAL SYRUP

4.

ARIFER SYRUP

5.

SEAGEM-L SUSPENSION

6. 7. 8. 9. 10.

NOVACID SUSPENSION CETEN SYRUP SUPAR SUSPENSION ARO SUSPENSION ARO-OZ SUSPENSION

50mg. PEPSIN(1:3000) I.P. 10mg. Each 5 ml contain. FERROUS GLUCONATE I.P. 300mg. CALCIUM GLUCONATE I.P. 125mg. CYANOCOBALMINE I.P. 10mcg. FOLIC ACID I.P. 1.5mg Each 5 ml contain. SODIUM FEREDETATE B.P. 231mg. FOLIC ACID I.P. 0.5mg. Each 5 ml contain. CALCIUM CARBONATE (OYSTER SHELL) I.P. 625mg. VITAMIN D3 I.P. 125 I.U L-LYSINE USP 70mg. Each 5 ml contain. MAGALDRATE I.P. 400mg. SIMETHICONE I.P. 20mg. Each 5 ml contain.
CETIRIZINE DIHYDROCHLORIDE BP

200 ML

200 ML

200ML

200ML

170 ML

5mg 50mg. 125mg. 50mg

60 ML 60 ML 60 ML 60 ML

Each 5 ml contain. NIMESULIDE B.P. PARACETAMOL I.P. Each 5 ml contain. OFLOXACIN . I.P. Each 5 ml contain. OLFLOXACIN I.P. ORNIDAZOLE Each 5 ml contain. OFLOXACIN I.P.

50mg. 125mg. 100mg.

11.

AROMET SUSPENSION

METRONIDAZOLE BENZOATE (EQ. TO METRONIDAZOLE) I.P. 200mg.

60 ML

12.

ARITONE SYRUP

Each 5 ml contain. CHLORPHENIRAMINE MALEATE I.P. 2.5mg. AMMONIUM CHLORIDE I.P. 125mg. SODIUM CITRATE I.P. 55mg. MENTHOL I.P. 1mg.

100ML

Each 5 ml contain.
DIPHENHYDRAMINE HCL I.P. 14.08mg.

13

ARYDRYL SYRUP

AMMONIUM CHLORIDE I.P. 138mg. SODIUM CITRATE I.P. 57.03mg. MENTHOL I.P. 1.14mg. Each 5 ml contain. BROMHEXINE HCL I.P. GUAIPHENESIN I.P. CETIRIZINE DIHYDROCHLORIDE B.P. MENTHOL I.P. Each 10 ml contain. SUCRALFATE USP OXETACAINE B.P. Each 5 ml contain. PARACETAMOL I.P. PHENYLPROPANOLAMINE HCL B.P. CHLORPHENIRAMINE MALEATE I.P.

100 ML

4mg. 50mg. 2.5mg. 1mg.

14.

BROX-CZ SYRUP

100ML

15

ARIFATE O SUSPENSION

1mg. 10mg.

100ML

125mg. 2.5mg. 1mg.

16.

NOCOLD SYRUP

100ML

17.

CYPOT SYRUP

Each 5 ml contain. CYPROHEPTADINE HCL . I.P. 2mg. TRICHOLINE CITRATE 0.275gm SORBITOL SOLUTION(70%) I.P. 3.575gm Each 5 ml contain. DISODIUM HYDROGEN CITRATE B.P. 1.53gm Each 5 ml contain. DEXTROMETHORPHAN HYDROBROMIDE I.P. 10mg. PHENYLPROPANOLAMINE HCL B.P 10mg. CHLORPHENIRAMINE MALEATE I.P 2mg. MENTHOL I.P. 1.5mg Each 5 ml contain. NIMESULIDE B.P. 50mg. PARACETAMOL I.P. 125mg. Each 5 ml contain. DRIED ALUMINIUM HYDROXIDE GEL I.P. SIMETHICONE I.P. Each 5 ml contain. OFLOXACIN . I.P. Each 5 ml contain. OFLOXACIN I.P. ORNIDAZOLE

200 ML

18.

CITRAL SYEUP

100 ML

19.

ARICOF SYRUP

100 ML

20.

NSP SUSPENSION

60ML

21.

ARICID SUSPENSION

200mg. 25mg. 50mg.

MAGNESIUM HYDROXIDE I.P. 200mg.

170ML

22 23.

OFCIN SUSPENSION OFCIN-OZ SUSPENSION

60 ml 60ML

50mg. 125mg.

24.

LIVOTOP SYRUP

Each 5 ml contain. CYPROHEPTADINE HCL . I.P. 2mg. TRICHOLINE CITRATE 0.275gm SORBITOL SOLUTION(70%) I.P. 3.575gm Each 5 ml contain. CHLORPHENIRAMINE MALEATE I.P. 2.5mg. AMMONIUM CHLORIDE I.P. 125mg. SODIUM CITRATE I.P. 55mg. MENTHOL I.P. 1mg. Each 10 ml contain. SUCRALFATE USP

200ML

25.

LCTONE SURUP

100ML

26. 27.

ARIFATE SUSPENSION PEPZYME SYRUP

1gm.

100ML

Each 5 ml contain. FUNGAL DIASTASE(1:1200) I.P. 50mg. PEPSIN(1:3000) I.P. 10mg Each 5 ml contain. FERROUS GLUCONATE I.P. 300mg. CALCIUM GLUCONATE I.P. 125mg. CYANOCOBALMINE I.P. 10mcg. FOLIC ACID I.P. 1.5mg Each 5 ml contain. CARBONYL IRON EQ. TO ELEMENTAL IRON 60mg. VIT. B12 I.P. 7.5mcg. FOLIC ACID I.P. 0.75mg. ZINC(as zinc sulphate I.P.) 11.25mg.

200ML

28.

CALCITONE-F SYRUP

200ML

29.

CARBOZ-SYRUP

200ML

1.6

Site Synopsis: The site is situated at Integrated Industrial Estate, Pant Nagar about 5 km away from Rudrapur city (Uttarakhand). It is accessible by rail as well as by road, about 237 km from Delhi, and about 300 km from Dehradun. The total area of the plot is approximately 1971.40 sq. yard. The plot is situated in pollution free environment.

1.7

Human Resource : Sr. No. 1. 2. 4. 5. 6. 7. 9. 10. 11 Department Production staff Quality Control Engineering Services Stores Administration Security House keeping Regulatory Operator Total Strength 04 03 02 02 03 02 05 01 05 27

2.0

PERSONNEL

2.1 LIST OF KEY TECHNICAL PERSONNEL AT PANTNAGAR SITE

Companys Responsible Person

Sr. No. Name Brief Biodata Designation - Managing Director/ Plant Head Education - B.Com Experience - Looking after the entire portfolio of Aries which includes the Sales, marketing, Legal & periodicals and manufacturing Designation - Production In-Charge Education - B.Sc Experience 7 years experience in production, Approved from Uttaranchal government in Tablet, Capsule & Liquid section Designation - QC In-Charge Education - B.Sc Experience 4 years experience in QC Department, Approved from Uttaranchal government in Chemical analysis Designation - Store In-Charge Education - B.Com Experience 3 years experience in store department

01

Mr. Amit Agarwal

02

Mr. Ashok Jaiswal

03

Mr. Kailash Dass

04

Mr. Anoop Dutta

2.2

Health Requirement : The company ensures that pre-employment and periodical medical check up is conducted for all employees.

2.3

Training Program : A detailed SOP for Training Program and a Training Manual is prepared by QC, in consultation with Plant head, HR and Departmental heads. This covers Induction training, On the job training, External training in cGMP, Health, Safety, Environment, personnel hygiene, instrumentation. The trainings conducted are documented and evaluated.

3.0
3.1

PREMISES, FACILITIES AND EQUIPMENT:

PREMISES: Manufacturing areas: Manufacturing facilities are segregated as per cGMP norms and separate buildings have been provided for Specialty Formulations, Oral Liquid Section.

3.2

Nature of construction and fixtures / fittings: Nature of construction : Brick & RCC External finish : Cement plaster with snowcem finish Internal Finish : The manufacturing areas are made up of a. Stone Flooring b. Polyurethane coatings on walls and ceilings. In other areas, Internal walls and ceilings are plastered with cement to smooth finish and painted with glossy washable antibacterial and antifungal paint. Peripheral areas, which are other than the production areas, are constructed by civil structure.

3.3

Water System (DM water) RO UNIT :- Model- INDRO-403 , MAKE ION EXCHANGE INDIA LIMITED. The water treatment system consists of treatment of water at various stages and passage through various filters as per the details given below: Bore well source is from artesian well designed to feed water Filtration through multi-grade filter Softener Antiscallent dosing RO Mix bed pH Stabilization Pass through UV. DM water

3.4

Distribution of DM Water: The distribution loops are made of SS with orbital arc welding and continuous flow of water with the provision of sampling points and user points, wherever required.

3.5

Preventive Maintenance: The preventive maintenance of the systems, building and premises including painting is carried out as per schedule. The ventilation and water systems are periodically serviced and checked for overall performance. Records are maintained as follows: The equipments are divided into a)
b)

Utility Equipments Production Equipments

Preventive maintenance documents are maintained separately. The schedule for preventive maintenance is formulated on annual basis for each manufacturing unit with specific break up of weekly / fortnightly / monthly / quarterly and half-yearly maintenance schedules. A list of major equipments and machinery used in production has been attached. 3.6 Validation and Calibration Validation Master Plan is prepared by QC in line with the philosophy of Aries Drugs Private Limited to plan and execute validation activities in the facility according to Validation Matrix. All critical equipments, instruments and utilities are subjected to followed by DQ, IQ, OQ and PQ. In case of any changes, revalidation is performed accordingly. Records are kept with detailed information for each equipment such as details of calibration standards and limits, responsibilities for performing calibration, intervals between calibration, record-keeping requirements and logs, and actions to be taken. The following validations are carried out: Water Validation Equipment Validation QC Instrument / Analytical Method Validation

Calibration of equipments by external agencies is carried out periodically and the tag indicating next calibration due is affixed on individual equipment.

3.7

SANITATION
Sanitation and Cleaning to ensure that the system is cleaned properly to be free from product, detergent and microbial flora to specified level to prevent contamination. Written guidelines and procedures for cleaning specifications, cleaning agents and their concentration to be used are available. In critical process areas, the equipments / machinery have been provided with CIP and SIP systems. Written SOPs are in place for cleaning and sanitization of manufacturing areas. which are Separate SOPs are available for cleaning of individual equipment / machinery, followed, & records are maintained thereof.

4.0
4.1

DOCUMENTATION
Documentation is an essential part of the Quality Assurance/Quality Control System. Its purpose is to define the system control and to specify / record various activities carried out and to ensure effective implementation. Documentation system includes the history for each batch of product. intermediate, bulk and finished products. Master documents such as Master Specification, Master Formula Card and Master File for each raw material, packing material and finished product are available with QA/QC department. It includes the

information on utilization and processing of starting materials, packaging materials and

5.0
5.1

PRODUCTION
Materials are procured from approved vendors against purchase order. The materials received at warehouse are cleaned free of dust by vacuum cleaner, checked for physical defects and kept in quarantine till QC sampling is done. After the QC Report, approved materials are shifted to Approved Area and if rejected, transferred to Rejected Materials Area. Rejected materials are kept under lock and key till they are returned to the vendor in case of raw materials and till they are destroyed, in case of printed packing materials. QC sampling and dispensing of raw materials is done under the specified areas. Dispensed materials are moved to Day Store till taken up for production. After production, the finished goods are maintained in the quarantine pending QC release. Once the QC release is obtained, the finished products are transferred to BSR. FACILITIES: Documentation (cGMP) Latest Equipment/Instruments for manufacturing. AHU with 0.5 filter. Fresh air system Cooling system Fresh air & AHU with 0.5 filter In Manufacturing & packing area.

5.2

Flow sheets

ORAL LIQUID PRODUCTION

BATCH MANUFACTURING RECORD

RAW MATERIAL REQUISITION (FORMULATION ORDER)

DISPENSING OF RAW MATERIALS

MANUFACTURING PROCESS

BULK

SAMPLING

TESTING QC RELEASE

IPQC

FILLING

PACKING MATERIAL REQUISITION

LABELING

IPQC

RELEASE FOR PACKING

PACKAGING

DISPENSING OF PM

SAMPLING & INSPECTION

QC RELEASE

TRANSFER TO STORE DEPARTMENT

5.3

LIST OF MAJOR EQUIPMENT AT PLANT

ORAL LIQUID SECTION S.NO. 1 NAME OF THE EQUIPMENT Sugar preparation tank with double Heater. (Capacity 750 Lit.) Manufacturing tank with stirrer and cooling facilities and In Line Homogenizer. ( Capacity 1000 Lit.) Filter Press Storage tank with stirrer ( Capacity 1000 Lit.) Rotary Bottle washing machine with air dryer Automatic four head Volumetric Liquid Bottle Filling machine Automatic four head Cap Sealing machine Automatic cap feeder machine Inspection table Labeling machine with vacuum system MAKE Pyramid Industries (Ahmadabad) Pyramid Industries (Ahmadabad) Pyramid Industries Pyramid Industries (Ahmadabad) Excel Engineering (Ahmadabad) MODEL

GMP Model

2 3 4 5 6 7 8 9 10

GMP Model GMP Model

ERWM-64 National Pharma Machinery NALF-100 National Pharma Machinery NARCS-100 National Pharma Machinery NARCS-100 Excel Engineering (Ahmadabad) EPCB Koldpack Machineries KHL-ISO P. Limited (Ahmadabad)

6.0

QUALITY CONTROL
Quality Control laboratories have been equipped with latest equipments & Instruments.

6.1

Quality control shall deal with sampling, specifications, testing, documentation, release procedure and ensure implementation of the relevant protocol The QC Lab has got the following sections: Chemical Instrumentation Packing materials testing Microbiology Re-agents and storage Control Samples Record Room Heating Equipments Area Stability Studies Wash Area FACILITIES General facilities The testing facility of analytical lab are designed as Instrumentation lab Chemical analysis lab Microbiology lab Specimen and data storage facilities Separate Room and cupboards are provided for storing the samples before and after analysis. All analytical data are entered in a prescribed protocol sheet based on which a test report is prepared. The data are filed according to the serial number of COA.

6.2

Administrative and personnel facilities All the administrative work related to the laboratory are supervised by QC In charge. Facilities for hand-wash and toilet are adequately provided.

6.3

Quality Management System: Our policy states: The commitment of the company is to ensure, that the products it develops, manufactures and distributes, meet the predetermined specification related to quality of its products consistently. It assures the products are manufactured in adherence to the current Good Manufacturing Practices (cGMP) in conformity with national regulations. The role of Quality Quality Control is to ensure design and development of pharmaceutical products taking into account the requirements of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP) Good Documentation Practices (GDP). Adequate controls on starting materials, bulk products and other in-process controls, calibrations and validations are carried out. The effective quality management is achieved through systematic sampling, testing, validating and monitoring of materials, facilities, systems and procedures, which can have direct impact on the quality of the products throughout their shelf life. Much importance is given to in-process controls on the guidelines given under Process The Standard Operating Procedures (SOPs), duly authorized for all operations including Production, Quality Control, Distribution, Safety, Environmental Control, Housekeeping and Engineering are the other important part of Quality Management System. Self-inspection and Audits are part of effective implementation of Quality Management System. Inspection, evaluation, rating and approval of vendors for supplies of raw materials, excipients and packing materials are carried out in conformity to the Good Manufacturing Practices.

6.4

LIST OF EQUIPMENTS / INSTRUMENTS IN QA/QC LAB Sr. No. 1. 2. 3. 4. 5. 6. 7 8 9 10 11 12 13 14 15 Equipment / Instrument Name UV-Vis. Spectrophotometer Refractometer K. F. Titrator Analytical Balance Polarimeter pH Meter Conductivity Meter Melting Point apparatus Muffle Furnace Hot air Oven Vacuum Oven Water Bath Hot plate Heating mantel UV Cabinet Systronics Advance EI Vibra Advance Toshcon Toshcon EI Shivaki J.S. Enterprises S.M. Scientific J.S. Enterprises J.S. Enterprises J.S. Enterprises J.S. Enterprises 117 R-8 761 HT-220E PA-1R CL 54+ TCM 15+ 931 T-701 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Make Model Qty

6.5 QC FLOW SHEET IN PROCESS AND FINISHED PRODUCTS ANALYSIS

DISPENSING

BULK SOLUTION

Description pH Fill volume Wt./ml Assay

TEST: 12PHARMACOPOEAL SPECIFICATIONS IN HOUSE SPECIFICATIONS

6.6

PACKAGING MATERIAL ANALYSIS AND RELEASE PRIMARY PACKAGING MATERIAL& SECONDARY PACKING MATERIALS PRIMARY SECONDARY

PET BOTTLE

PP CAP

LABEL

CARTON

CORRUGATED BOX

PHYSICAL DIMENSIONS

PHYSICAL DIMENSIONS

PHYSICAL DIMENSIONS

PHYSICAL DIMENSIONS

PHYSICAL DIMENSIONS

CHEMICAL TESTING

CHEMICAL TESTING

CHECKING OF PRINTED MATTER

CHECKING OF PRINTED MATTER

GRAMMAGE & PRINTED MATTER

COMPLIES

COMPLIES

COMPLIES

COMPLIES

COMPLIES

RELEASE

RELEASE

RELEASE

RELEASE

RELEASE

7.0

STORE DEPARTMENT
General facilities Documentation Separate Under Test area with yellow coloured mark on floor. Separate Approved area with Green coloured mark on floor. Separate Rejected area with Red coloured mark on floor. Cooling area Dispensing & Sampling Booth with LAF Cold storage area for Multivitamins and other raw material. Finish goods storage area. Primary & Secondary Packing materials area.

8.0

CONTRACT MANUFACTURE & LICENSE SHEET

The Contract Manufacturing can be undertaken on either as Loan License or principle to principle (P to P) basis. In P to P basis- All the materials shall be arranged by the manufacturer & License shall also be arranged by manufacturer under the brand name of marketing company. The Loan License- Under the Loan license The Manufacturing is done with the materials supplied by the Licensee & the license for the manufacturing is to be arranged by the marketing company at our premises. All the manufacturing activities are done under strict supervision of technical staff following latest cGMP norms.

9.0

DISTRIBUTION, COMPLAINTS AND PRODUCT RECALL

Warehousing areas are designed and good storage and distribution practice are adopted. The areas are maintained within acceptable temperature limit. Controlled storage condition is monitored constantly. Distribution details are maintained batch wise to facilitate recall of goods, if required.

9.1

Handling of Complaints and Product Recalls A Standard Operating Procedure is available for the handling of complaints and Product Recall Procedure is in place. Complaints will be investigated by QC department as per written

procedure and the QC Manager instructs further action / recall.

9.2

SELF-INSPECTION
Periodical internal audits (self inspection) are carried out as per the SOP of Internal Audit. Internal audit is either conducted by the internal audit team or by authorized QA/QC personnel. Internal auditors, who form the audit team, are selected from various departments except the auditee department. The auditors prepare internal audit reports and the concerned Department Head is required to submit the corrective action plan. External experts are also called periodically to evaluate our working on the principles of GMP, GLP, GDP.

10.0 ORGANIZATION CHART: ORGANOGRAM OF PANTNAGAR SITE Mr. HARIOM AGARWAL CHAIRMAN

Mrs. MUKUL AGARWAL (MARKETING DIRECTOR)

Mr. AMIT AGARWAL (DIRECTOR & PLANT HEAD)

Mr. SUSHANT RAI AGRWAL (H.R & ADMINISTRATION.)

Mr. ROBIN MATHEW (DIRECTOR)

MARKETING MANAGER

MEDICAL REPRESENTATIVES

Mr. ASHOK JAISWAL (PRODUCTION INCHARGE)

Mr. KAILASH DASS (QC INCHARGE)

DISTRIBUTORS

Mr. ANOOP DUTTA (STORE INCHARGE)