Info@visiondrugs.co.in 040-4005 1090/1088/1048

Overview:

Vision Drugs Pvt Ltd. is established in 2008 by a team of industrialists with a passion towards manufacturing of pharmaceutical bulk drugs. In our journey of more than a decade we have handled many niche molecules and have emerged as one of the reputed manufacturing company in the industry. Our determination has driven us from a development lab to a commercial scale Intermediates/APIs manufacturing company. Our strength lies in our strong process chemistry and focus on retro synthesis which enabled us to meet the global pharma requirements. We believe human resource is our best competency who are dedicated and determined for the betterment of the organization. As a rapidly growing company we ensure a strictly implement “SHE” policy.

Our Mission & Vision:

Vision

"To Emerge as leading Indian Pharmaceutical company meeting global healthcare needs by providing superior research driven value to our customers through innovation, focus & specialization"

Mission

“Develop, produce & deliver high quality advanced drug intermediates & pharmaceutical active ingredients for the global pharmaceutical industry "

Quality Management System

Quality Management System at Company comprises three primary departments - Quality Assurance, Quality Control and Regulatory Affairs. The role of each department is designed in such a way that each of them counter checks the manufacturing activity and ensures the strict quality practices as per the regulatory standards. VISION has established stringent Quality practices in accordance with Schedule M and ICH Q7 as per cGMP.

Quality Assurance

Company’s Quality Assurance is responsible for the site-specific maintenance, compliance, realization and further development of internal Quality Management Systems. Quality Assurance ensures that API's and Advanced Intermediates produced from various stages of manufacturing to comply with cGMP requirements. Following are few of the important activities handled by Quality Assurance team.

  • Document control & Annual Product reviews.
  • Monitoring of all validations including cleaning validations.
  • Change control compliance, batch release & product recall.
  • In-process and retrospective audits.
  • GMP training.

Quality Control

A well-equipped advanced lab for precision and ruggedness of the quality testing according to the pre-determined MOA as per pharmacopeia or in-house developed and validated analytical methods, we have experienced professionals heading the department and well-qualified employees performing the analysis in compliance with the ICH guidelines. The key responsibilities of QC are:

  • Raw material Analysis & Approval.
  • Batch Analysis & Approval.
  • Retaining samples (Control samples & stability samples).

Regulatory Affairs:

Highly competent team of professionals with a good knowledge of regulatory guidelines, the team is headed by a well experienced professional with expertise in regulatory filing, DMF compilation, product registration, agency registrations and regulatory training. Our RA team is always in direct reach to our customer for timely support.