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Quality

Company Factsheet

Nature of Business: Manufacturer
Total Number of Employees: Upto 10 People
Year of Establishment: 1986
Legal Status of Firm: Limited Company (Ltd. / Pvt. Ltd.)
Annual Turnover: 2014-15 Rs. 500 - 1000 Crore Approx.
GST No.: 03AABCI1842A1ZF
CIN No.: L24116PB1986PLC007030

Quality Policy

We at IOL Chemicals and Pharmaceuticals Ltd., are committed to supply good quality products, excelling laid down standards to delight our customers by continually upgrading our skill, technology, processes and complying to Good Manufacturing Practices and Quality Management Systems.

Varinder Gupta
Chairman & Managing Director
Rev. No. 01
Eff. Dt. 13.03.2008

Quality Mantra

IOL’s quality supervision is demonstrated at all phases of product life cycle. Quality supervisor begins evaluation with careful documentation. This ensures compliance with good laboratory practices and consequently integrity of the data produced. Quality supervision is continued for production, distribution and conclusion for shelf life of product

Quality Policy
We at IOL Chemicals and Pharmaceuticals Ltd., are committed to supply good quality products, excelling laid down standards to delight our customers by continually upgrading our skill, technology, processes and complying to Good Manufacturing Practices and Quality Management Systems.

System and procedures
All the procedures are prepared, reviewed and approved and after imparting training to all concerned these procedures are made effective. Systems are in place for processing, analysis and release of all finished products of the company.

Support to validation and qualification Validation is executed for all processes including process, analytical and cleaning methods whereas qualification is executed for all support services like utilities, equipments and water systems as per ICH guidelines and supporting documentation is maintained.

Deviation and change control monitoring
All unplanned events are categorized as deviations and record for these events is maintained and corrective and preventive actions are derived to avoid repetition of these events. All the changes related to processing, analysis or documents are routed through change control and records for all change controls is maintained.

Documentation control
Documentation of the company is controlled as per sop “ control of documents” and all the activities related to documentation are followed according to SOP. Activities like preparation, control and issuance of the documents is maintained strictly as per the SOP.

Quality Assurance

Quality Control LaboratoryThe Quality control lab has well equipped instruments like:

Quality Compliance

Ensuring adherence to IOLCP’s quality standards is the responsibility of its dedicated Corporate Quality Assurance team. The team(s) charter includes enforcing a standardized common quality system across the organization to ensure consistency, effectiveness and efficiency during the manufacture of its products.
S.No.CertificationDownloads
1.ANVISA issued by Brazilian Authorities

 

2.Certificate of Suitability from European Directorate for the Quality of Medicines (EDQM)

 

3.Eu/Dir/62 approval issued by CDSCO Authorities, India

 

4.Certificate of Pharmaceutical Products (COPP), WHO issued by Directorate of Health and Family welfare

 

5.EUGMP certification issued by Hamburg Authorities Germany

 

6.PMDA, Japan issued by Ministry of Health, Japan

 

7.Drug Administration Bangladesh by Ministry of Health, Bangladesh

 

8.Ministry of Health approval,Iran

 

9.GMP Certificate issued by Directorate of Health and Family Welfare(State Governement)

 

10.Ministry of Health approval,Phillipines

 

11.Ministry of Health approval,Ukrain

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    Vijay Garg

    (Joint Managing Director)

    IOL Chemicals And Pharmaceuticals Limited

    Industrial Area- A, Ludhiana, Punjab, India

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