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April 2016
Cross Contamination: Source and Prevention – 2Days Training Programme
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 critical and most objectionable incident in food, chemicals, agro products ,APIs and formulation manufacturing industries . Historical events are evident to claim hundreds of fetal…
Find out more »Industrial Hydraulics Basics – Full Day program from QCFI Pune
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 become a way of life as most of the applications have some form of system ingrained.Hydraulics is a type of science and engineering that deals with…
Find out more »A New Approach to Process Validation – 2Day Training Programme
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 - Risk Management - Quality System tools and management. A New approach to Process Validation has been linked with a “Product life cycle concept” which includes…
Find out more »May 2016
Concepts of cGMP – Two Day Training Programme at Surat
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 : Objective of this training programme is to guide participants to current Good Manufacturing Practices during manufacturing of pharmaceuticals. CERTIFICATE : Certificate will be awarded to…
Find out more »August 2016
Awareness Session on Lean Manufacturing for Productivity Enhancement
Dear all, CII Mysuru in Partnership with QCFI Mysuru Chapter is organizing an Awareness Session on Lean Manufacturing for Productivity Enhancement in Automotive Axles Ltd Please depute your persons for this program who can take decision trailing mail are the details of the program. Please send us the confirmation of your participation. Thanks . ABDUL KAREEM. Jont secretary QCFI Mysuru chapter Mobile :- 09886015757 Awareness Session on Lean Manufacturing for Productivity Enhancement 1600 – 1730 Hrs. 4th August 2016: Automotive Axles…
Find out more »4 Days Workshop on “Training for Trainers” – QCFI Delhi Chapter – Headquarter
Workshop on “Training for Trainers
Find out more »TWO DAYS TRAINING PROGRAM – QCFI Ankleshwar Chapter & Surat Sub Chapter
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 cycle approach and system promoting continual improvement. OBJECTIVE : An objective of this training program is to explain this guideline in Global Approach. CERTIFICATE :…
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One Day Training Prog. on “Application of Minitab for Data Analysis
QCFI Chennai - Minitab Programme Brochure Aug -2016
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