Introduction: Download Brochure A revised guidance on A New Approach to Process Validation published in Jan. 2011, provides recommendations that reflect some of goals of FDA’s initiatives entitled “Pharmaceuticals GMP for the 21st Century, A Risk-Based Approach”, particularly with regard to the use of. * Technological advances in Pharmaceutical manufacturing. * Implementation of a - […]

INTRODUCTION : FDA insists  compliance of cGMP while manufacturing of pharmaceuticals. Also, compliance of cGMP ensures satisfaction to stakeholders (patients). it has  been a  mandatory requirement that  persons involved  in manufacturing of pharmaceuticals should be adequately trained for cGMP, as compliance of cGMP is a responsibility of all the persons involved in manufacturing. OBJECTIVE : […]

  QCFI had discussion with Manager, International Relations, Office Secretariat and finalised long term deal with JUSE at special rate to Indian delegates for study Tour to Japan. Executives from Indian industries have a golden opportunity to visit Japanese industries and learn their ways to implement in your own organization for the world class performance. […]

Workshop on “Training for Trainers

TWO DAYS TRAINING PROGRAM ON GOOD MANUFACTURING PRACTICES WITH GLOBAL APPROACH TO RISK MANAGEMENT & CONTINUAL IMPROVEMENT INTRODUCTION : Good Manufacturing Practices intended to provide guidance regarding cGMP for manufacturing of API and intermediates. Considering the needs of system for 21st century, this guideline should be implemented in accordance with the current approaches of Risk Management, Life […]

                      Aurangabad-CCQC-2016-Brochure                                CCQC - 2016 Report

QCFI Chennai - Minitab Programme Brochure Aug -2016