Institute of Good Manufacturing Practices India, registered as a non-profit society with Government of India and a member (as a higher/professional Education Institute) of Quality Council of India(QCI) -which is an autonomous body and an accreditation authority for education & vocational training providers under the Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India -presents unique, friendly and interactive platform to get rid of all your GMP related glitches. GMP- is an essential element of industries like pharmaceutical, cosmetic, Ayurveda, biotech, homeopathic, medical device and food manufacturing. GMP in itself is the most dynamic part which witnesses frequent changes in terms of newer rules being added and older ones being renewed. Keeping self updated with current GMPs thus becomes inevitable to stay abreast with the changing industry needs and practices.
Our group of learned professionals from above mentioned sectors of the pharma and healthcare industries have put together their knowledge; know about and practical experiences in form of this GMP guide. IGMPI is moving hand in hand with technology advances and has gained recognition as stronger and better training & distance and e-learning platform provider for pharmaceutical and healthcare professionals in the aeas of GMP, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice and Product Management. The importance of quality healthcare is known to our founders and thus numerous efforts are being made to offer friendly but effective and easy online/distance sources of GMP information, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice in form of online seminars, distance/online courses as well as training programmes along with knowledge of worldwide affairs of the industry; in short a round-the-clock help for any information in these areas needed by anybody from around the world. Based on high standard of quality, the training programmes in Pharma and healthcare GMP, Quality Assurance and Quality Control, Regulatory Affairs, IPR, Pharma Product Management etc areas have been approved and certified by Quality Council of India.
The IGMPIs team of technology experts and other Industry advisors together pursue to make cGMP knowledge, training in the area of Pharma and healthcare manufacturing easily accessible, through this platform.
Campden BRI and Alchemy in partnership with BRC, SGS, SQF and TSI have released the results of the fourth annual global survey of food safety training. The survey questioned food and drink manufacturers and processors worldwide to identify the needs, effectiveness and challenges of food safety training in the industry.
The results reveal some interesting trends:
Improving food safety culture was the top training goal for almost 80% of those surveyed
Many companies are not exploiting the specialist expertise available in their HR departments
Traditional training methods are still favored over online methods
Institute of Good Manufacturing Practices India, registered as a non-profit society with Government of India and a member (as a higher/professional Education Institute) of Quality Council of India(QCI) -which is an autonomous body and an accreditation authority for education & vocational training providers under the Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India -presents unique, friendly and interactive platform to get rid of all your GMP related glitches. GMP- is an essential element of industries like pharmaceutical, cosmetic, Ayurveda, biotech, homeopathic, medical device and food manufacturing. GMP in itself is the most dynamic part which witnesses frequent changes in terms of newer rules being added and older ones being renewed. Keeping self updated with current GMPs thus becomes inevitable to stay abreast with the changing industry needs and practices.
Our group of learned professionals from above mentioned sectors of the pharma and healthcare industries have put together their knowledge; know about and practical experiences in form of this GMP guide. IGMPI is moving hand in hand with technology advances and has gained recognition as stronger and better training & distance and e-learning platform provider for pharmaceutical and healthcare professionals in the aeas of GMP, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice and Product Management. The importance of quality healthcare is known to our founders and thus numerous efforts are being made to offer friendly but effective and easy online/distance sources of GMP information, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice in form of online seminars, distance/online courses as well as training programmes along with knowledge of worldwide affairs of the industry; in short a round-the-clock help for any information in these areas needed by anybody from around the world. Based on high standard of quality, the training programmes in Pharma and healthcare GMP, Quality Assurance and Quality Control, Regulatory Affairs, IPR, Pharma Product Management etc areas have been approved and certified by Quality Council of India.
The IGMPIs team of technology experts and other Industry advisors together pursue to make cGMP knowledge, training in the area of Pharma and healthcare manufacturing easily accessible, through this platform.
Campden BRI and Alchemy in partnership with BRC, SGS, SQF and TSI have released the results of the fourth annual global survey of food safety training. The survey questioned food and drink manufacturers and processors worldwide to identify the needs, effectiveness and challenges of food safety training in the industry.
The results reveal some interesting trends:
Improving food safety culture was the top training goal for almost 80% of those surveyed
Many companies are not exploiting the specialist expertise available in their HR departments
Traditional training methods are still favored over online methods
Pharmaceutical industry is a very vital segment of the
our health care system, which deals with manufacturing
and marketing of pharmaceuticals and biological
products and medicinal devices, used for the diagnosis
and treatment of diseases as well as conducts research
for development of new products for human welfare
TQM involves
building quality in a pharmaceutical product as it
involve complete records such as standard operating
procedures for every step, validation records, master
formula records and batch production records etc.
“A GMP is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product”.
Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
Good Manufacturing Practice is a set of regulations, codes, and guidelines for the manufacture of drug substances and drug products, medical devices, in vivo and in vitro diagnostic products, and foods.
Pharmaceutical industry is a very vital segment of the
our health care system, which deals with manufacturing
and marketing of pharmaceuticals and biological
products and medicinal devices, used for the diagnosis
and treatment of diseases as well as conducts research
for development of new products for human welfare
TQM involves
building quality in a pharmaceutical product as it
involve complete records such as standard operating
procedures for every step, validation records, master
formula records and batch production records etc.
“A GMP is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product”.
Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
Good Manufacturing Practice is a set of regulations, codes, and guidelines for the manufacture of drug substances and drug products, medical devices, in vivo and in vitro diagnostic products, and foods.
Institute of Good Manufacturing Practices India, registered as a non-profit society with Government of India and a member (as a higher/professional Education Institute) of Quality Council of India(QCI) -which is an autonomous body and an accreditation authority for education & vocational training providers under the Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India -presents unique, friendly and interactive platform to get rid of all your GMP related glitches. GMP- is an essential element of industries like pharmaceutical, cosmetic, Ayurveda, biotech, homeopathic, medical device and food manufacturing. GMP in itself is the most dynamic part which witnesses frequent changes in terms of newer rules being added and older ones being renewed. Keeping self updated with current GMPs thus becomes inevitable to stay abreast with the changing industry needs and practices.
Our group of learned professionals from above mentioned sectors of the pharma and healthcare industries have put together their knowledge; know about and practical experiences in form of this GMP guide. IGMPI is moving hand in hand with technology advances and has gained recognition as stronger and better training & distance and e-learning platform provider for pharmaceutical and healthcare professionals in the aeas of GMP, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice and Product Management. The importance of quality healthcare is known to our founders and thus numerous efforts are being made to offer friendly but effective and easy online/distance sources of GMP information, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice in form of online seminars, distance/online courses as well as training programmes along with knowledge of worldwide affairs of the industry; in short a round-the-clock help for any information in these areas needed by anybody from around the world. Based on high standard of quality, the training programmes in Pharma and healthcare GMP, Quality Assurance and Quality Control, Regulatory Affairs, IPR, Pharma Product Management etc areas have been approved and certified by Quality Council of India.
The IGMPIs team of technology experts and other Industry advisors together pursue to make cGMP knowledge, training in the area of Pharma and healthcare manufacturing easily accessible, through this platform.
Shamisha Learning Center, Ahmedabad, Gujarat, India-Specialized Training, Workshops and courses on Quality, Regulatory, R & D, Supply Chain and Manufacturing
Quality Management System including the Quality management and certificationAshwiniRaikar1
Concept of Quality, Total Quality Management, Quality by Design, Six Sigma concept, Out of Specification, Change control, Introduction to ISO 9000 Series of quality system standards, ISO 14000,NABL, GLP
Audit training
Introduction in Registration
Introduction in QMS
Good Manufacturing Practices (GMP)
Good Distribution Practices (GDP)
Good Laboratorical Practices (GCP)
Introduction in Validation Basics
Acceptance Sampling
Design of Experiment (DoE)
Quality by Design (QbD)
GAMP5
Intro Serialisatie
Tech Transfer
ISO 13485 – Medical Device
1. Post Graduate/ Executive Diploma in
Pharmaceutical Good Manufacturing Practices
Approved and Certified by Quality Council of India, Government of
India
Institute of Good Manufacturing Practices India
B-271, Chattarpur Enclave Phase-2, 100 Feet Road,
Chattarpur, New Delhi-110074 (India)
Telephone: +91 8130924488,+91 11 65353339
E-mail: info@igmpiindia.org
2. About IGMPI
Institute of Good Manufacturing Practices India, registered as a non-profit society
with Government of India and a member (as a higher/professional Education
Institute) of Quality Council of India(QCI)-which is an autonomous body and an
accreditation authority for education & vocational training providers under the
Department of Industrial Policy & Promotion, Ministry of Commerce & Industry,
Government of India -presents unique, friendly and interactive platform to get rid
of all your GMP related glitches. Based on high standard of quality, the training
programmes in Pharma and healthcare GMP, Quality Assurance and Quality
Control, Regulatory Affairs, IPR, Pharma Product Management etc. have been
approved and certified by Quality Council of India.
3. IGMPI Work Ideology
IGMPI’s work ideology remains
“When outcome matters wise integration of
knowledge and technology becomes essential to
promote best results.”
4. Good Manufacturing Practices: Its
importance creates its need!
Good Manufacturing Practices (GMP) is
the most talked about tool of utmost
importance in manufacturing world today.
GMP is set of principles and procedures
that are followed by manufacturers to
ensure that the products are consistently
manufactured as per the specifications.
The preambles of GMP target to cover all
areas and characteristics of any
production method which can affect the
quality of final product. GMP and its
application is not restricted to
manufacture of solely pharmaceutical
drugs but extends to variety of other
products like food supplements,
cosmetics, medical devices, health
supplements and alternate healthcare
products like medicinal oils, ointments
etc.
Hygiene in
production
Quality
management
Suitable
facility
Qualified
personnel
Regulatory
documentation
Complaints
and recalls
GMP
5. Course Modules
Module 1: Good Manufacturing Practices and Its Regulations
Module 2: Qualification and Validation
Module 9: Deviation Management, CAPA and Change Control
Module7: Basics of Contract Manufacturing and Analysis
Module 5: Concept of Quality in Pharmaceutical Industry/Drug Discovery
Module 3: Good Documentation Practices and Record Keeping
Module 10: Good Manufacturing Practices for Active Pharmaceutical Ingredient
Module 8: Compliant Handling and Product Recall
Module 6: Conducting and Facing Self-Inspection and Quality Audits
Module 4: Manufacturing Operations and Controls in Pharmaceutical Industry
Module 12: GMP in other industries apart from Pharma
Module 11: The Indian GMP Regulation
Module 13: Case Studies
6. About Programme
Eligibility: Any Graduate/ Post graduate/ PhD (Post Graduate Diploma)
Any working professional with 6 months of experience
(Executive Diploma)
Post Graduate Diploma in Good Manufacturing Practices: 12 months
(Regular/ Distance)
Executive Diploma in Good Manufacturing Practices: 6 months (Part-
time/ Distance)
Fees:
Regular: Rs 1,35,000 /- Programme fee, Rs 3,000/- Examination fee.
Part-Time: Rs 70,000 /- Programme fee, Rs 3,000/- Examination fee.
Distance cum e-learning: Rs 14,000/- Programme fee, Rs 300/- per module
Examination fee.
7. Objective of the Programme
•To make professionals familiar with the changing faces of the
industry, upcoming issues, latest industry news and related
changes in the regulations, new compliance rules and much
more stands strong.
•To provide ample experience in GMP regulations regarding
manufacturing, storage and distribution, working environment,
documentation for participants to garner the required
exposure.
•It provides overview of practical situations and case studies
along with changing guidelines and compliance rules.
8. •To provide all knowledge and information about GMP, basics,
history, formulation and application strategy, compliance,
marketing rules, regulatory authorities and other Good
practices and their application in varied industry types.
9. GMP: Widest application zone
among all business and
industry types!
Those with GMP specific knowledge fit perfectly as part of and even lead quality
assurance, production process management, regulatory compliance and
packaging process teams in the major manufacturing units, where GMP
compliance is a must. After completing this course, the student can work as:
•Production Manager
•Quality Assurance Manager
•Quality Audit & Compliance Specialist
•Quality Documentation Team Leader
•Quality Supervisor
The students can ensue their career in Pharma, Healthcare, Ayurvedic,
Homeopathy, Food manufacturing or any related industry.
10. Placement Assistance
Professional resume writing
Providing interview skills
Conducting mock interviews
No extra fee for placement programme
Associated with many Pharma and Healthcare
industries
11. Participation from the Industry
In recent months the Institute has witnessed more and more participation from
professionals working with
12. For more details/counseling, you can call/write us: at +91 8130924488,
+91 11 65353339 & programmes@igmpiindia.org