Quality Control, Quality Assurance & Basic GMP Trainings
In depth & detailed training program in Quality Control which can make you well trained to work in Quality Control department. In this program you will learn about the different aspects of Quality Control department in a Pharma Company. It constitutes 16 training modules, 3 Assignments & 7 Assessments. The total duration of training is 22 hours.View Details
This is a 28 hours detailed training program for Quality Assurance. It includes 20 modules, 10 Assessments & 6 Assignments. This program is designed in alignment with the latest regulatory principles, guidelines & requirements to keep you updated. Once you go through this interactive program, you will be feeling more confident to work in any quality assurance department z7 the chances of your promotion will increase due to extensive knowledge & practical work approach.View Details
This program constitutes 8 training modules for a total of 14 hours duration. It constitutes 5 Assessments & 4 Assignments. The course contains in depth training on Pharmaceutical Quality Systems, Premises & Equipments of OSD/API, Material management, Warehouse managements, Quality Control Lab, Acts & Regulations and much more...View Details
Know Your Educator
Sunil SinghGMP & Compliance Specialist
Sunil Singh has given 25 years of his life perfecting the art of upholding the highest possible standards of medicine quality. Graduating with M.Sc. in Organic Chemistry in 1994 from Banaras Hindu University (BHU), he has discharged numerous responsibilities during his career like handling of regulatory and customer audits, people development through training and demonstration, implementation and monitoring of Quality Systems based on FDA’s six quality systems approach, preparation of corporate guidelines for implementation across other sites in the organisation, monitoring the stability of API and DF, monitoring of Quality Systems through Quality Metrics as per new FDA/ MHRA guidelines and improving the productivity of QC labs by streamlining processes and removing bottlenecks in the system. He has been instrumental in the implementation of GMP/ Quality systems in compliance with guidelines/regulations like Schedule M, ICH Q7, USFDA, MCA, TGA, ANVISA, MCC, WHO, 21 CFR Part 210 & 211 etc. Handling of change control, Product complaints, response to regulatory audits, batch recall, CAPA, investigation, deviation management from set parameters/ regulations, OOS and Risk management. He has audited more than 75 plants that handle Drug Formulation, API, Intermediate and Packaging Material manufacturing. He has also handled Third Party manufacturing sites and ensuring timely batch release while making sure the required regulations are met. He has also effectively handled more than 50 inspections by reputed customers and regulatory agencies like USFDA, TGA, MCC, WHO, ANVISA, IMB, Ministry of Health (Russia) successfully. His core skills include Training and Development based on cGMP guidelines and regulations, Audit and compliance, Mentoring and Quality management system design and their effective implementation. Unflinching in resolve and surprisingly simple and logical in approach. He has started his career with Lupin and worked with organisations like Matrix Laboratories, Mylan Pharmaceuticals, Aurobindo Pharma, Ranbaxy, Sun Pharma, Dabur Pharma, Dr. Reddy’s Laboratories and Jubilant Generics.