Two Days Training Programme (Non-Residential) Cross Contamination: Source and Prevention Download Brochure Faculty: Dr.Milin Pathak Organized by: Quality Circle Forum of India Ankleshwar Chapter & Surat Sub Chapter Venue: Hotel Lords Plaza Station Road, Surat. Date: 22nd - 23rd April Time: 9:00 AM to 5:00 PM Introduction: Mix-up, contamination and cross contamination has been considered […]

Quality Circle Forum of India - Pune Chapter.  Presents Full Day program on “Industrial Hydraulics Basics” on Thursday 28th April 2016 Timing : 9.00 am to 5.30 pm ( Registration & Breakfast 9:00 am to 9:30 am) At Quality Circle Excellence Centre Plot No: J/P-10,  Ganeshnagar , Telco Road, MIDC Bhosari, Pune 411 026 Today Hydraulics has […]

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 […]