Quality

Company Factsheet

Nature of Business: Manufacturer
Total Number of Employees: Upto 10 People
Year of Establishment: 1991
Legal Status of Firm: Limited Company (Ltd./Pvt.Ltd.)
Annual Turnover: Rs. 10 - 25 Crore
DGFT / IE Code: 3399001983
GST No.: 09AABCA6213B1ZA
CIN No.: U24112UP1987PTC008667

Quality Control

Quality Control
STERILITY 
All drugs are provided with air locks, dust free, ventilated with air supply. Access to the manufacturing area is restricted to authorized personnel. 

» WORKING SPACE 
Adequate working space and adequate room for orderly placement of equipment and materials is provided to eliminate any risk of mix up between different formulations and cross contamination. In storage area separate space is provided for under test, approved and rejected materials. 

» HEALTH, CLOTHING AND SANITATION OF WORKERS 
All the personnel coming in direct contact with the products including raw materials are always free from contagious and obnoxious diseases and they undergo periodic health check up. Just before entry to the manufacturing area change room with facility for personnel cleanliness etc is provided. 

» MEDICAL SERVICES 
We have provided-
(i) Adequate facilities for the first aid 
(ii) Medical Examination of worker at the time of employment and periodic check up thereafter time to time 
(iii) Facility for vaccination or other exigencies, We have provide service of a qualified physician for assessing the health status of personnel involved in the manufacturing and quality control of drugs is also made available. 


» SANITATION IN THE MANUFACTURING PREMISES 
The manufacturing area is not be utilized for any other purpose and it is maintained clean and in an orderly manner, free from accumulated waste, dust, debris etc. We always draw up and observe a routine sanitation programme. 

» EQUIPMENTS
All equipments used for the manufacturing of drugs are constructed, designed, installed and maintained in a manner so that they minimize the contamination like physical, chemical or Physico-chemical contamination. 

» RAW MATERIALS 
All raw materials are 
(i) Identified and their containers are examined for damage and assigned control number. 
(ii) Stored at optimum temperatures and relative humidity. 
(iii) Systematically sampled by quality control personnel, these are checked for compliance with required standards of quality. 

» MANUFACTURING OPERATIONS AND CONTROLS
All manufacturing operations of our factory are carried out under the supervision of competent technical staff. All vessels, containers and mechanical manufacturing equipment are conspicuously labeled with the name of the product and batch no. etc. 

» PRODUCT CONTAINERS AND CLOSURES 
All containers and closures are complied with the pharmacopoeial requirements. These are non reactive (inert) in nature. 

» QUALITY CONTROL SYSTEM 
We have separate quality control department which is supervised by many approved expert staff. Our quality control laboratory checks and controls the quality and stability of raw materials as well as finished goods.
Our quality control laboratory has the following principal duties:- 

(i) To prepare detailed instructions in writing for carrying out each test and analysis. 
(ii) To release or reject 
     (a) each batch of raw materials
     (b) Semi-finished products
     (c) packaging and labeling materials and the final container in which drugs are to be packed.
 





Our Quality Assurance

Our Quality Assurance
We always determine and follow that the product meets all the applicable specifications and that it is manufactured according to international standards and the GMPs (Good Manufacturing Practices). 

Our department of quality control is staffed with scientists and technicians responsible for the analytical testing of incoming raw materials and inspection of packaging components, including labeling. They conduct in-process testing where required, perform environmental monitoring and inspect operations for compliance, finally, they conduct the required tests on the finished dosage form. 

Our Quality Control is responsible as part of its testing and inspection functions, for monitoring the environmental conditions under which products are manufactured and/or held. 

The technical team is assisted installation of most modern and sophisticated instruments such as:.

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    Anuj Arora

    (Managing Director)

    Arosol Chemicals Private Limited

    Saharanpur Industrial Area, Saharanpur, Uttar Pradesh, India

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