Quality Policies

Quality Management System

Company to be strictly follows current good laboratory practices access the quality assurance system within the company.

Site quality consists of two parts, Quality control and Quality assurance. Both department headed by the Quality head who reports directly to the company partners.

Self Inspection

Audit program or self inspection is implemented with aim to evaluate the effectiveness of applied quality system and ensuring that every step of analytical process is according to GLP principal.

QA has written program to review the result of analysis periodically as per SOP and necessary corrective action are taken.

Training

  • All employee are given basic training on GLP , hygiene and safety , On job training are also given by trained personnel If required retraining also given after evaluation.
  • There are different types training program designed for different level of employee.
  • For need base topics in house training are conducted by external/ in-house trainer.
  • Personnel Hygiene Requirement including Clothing.
  • All employee are provided with company apron, hand gloves caps , mask , safety goggles etc., arrangements are made for getting the apron washed laundered regularly.

The quality of the offered industrial chemicals is checked on different parameters such as:

  • Observing the most rigid quality control standards at all the stages of manufacturing
  • Using ultramodern and well maintained machinery and testing equipment
  • Regularly reviewing our standards and processes to meet the specific requirements of our clients
  • We have fully equipped laboratories for ensuring that quality control standards are adhered to
  • Our professionals ensure that only quality certified goods leave the plant

Responsibility of quality Assurance

  • Approval of art work.
  • GLP enforcement, internal audit and training.
  • Controlling standard operating procedure.
  • Implementation, validation and calibration of the equipment.
  • Analytical method and method validation.
  • Complaint handling and support of the regulatory affairs.
  • Documentation.

Certifications