Home Manufacturing Facility
IOLCP, a leading manufacturer of Active Pharma Ingredients and
Specialty chemicals operates its manufacturing facilities from Barnala
(Punjab). The state of the art facilities as per current GMP guidelines
spread over 56 Acres of land at single location.
The site was chosen to manufacture API in batch manner while Intermediates and specialty chemicals are manufactured under continuous product delivery for vertical integration into dedicated product manufacturing facility.
There are 3 stand-alone blocks which are involved in manufacturing of APIs, key pharmaceutical Intermediates and Specialty Chemicals. Plants are designed as per current GMP requirements and clean rooms for finish products are provided with ISO class-8 HVAC system. Key pharmaceutical intermediates and specialty chemical plants are DCS controlled continuous process plants. All plants are designed as per latest technology and ISO standards.
Quality Operations include stand-alone facility for Quality Assurance, Quality Control & Microbiology Labs.
Four stage treatment zero discharge ETP, Solvent Recovery Plants & EHS cell is within the premises.
Dedicated power generation plant of 17MW catering to entire API, KPI and chemical blocks.
All manufacturing plants are provided with dedicated decentralized utilities from -20 to 275 deg.C. temp. Systems are operated based on the requirement of the process.
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
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 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.