1. Introduction
Good Manufacturing Practices (GMP) are a set of principles and guidelines that ensure products are consistently produced and controlled according to quality standards. They are designed to minimize risks involved in pharmaceutical, food, cosmetic, and medical device manufacturing that cannot be eliminated through testing the final product alone.
GMP covers all aspects of production — from raw materials, premises, and equipment to staff training, hygiene, documentation, and quality control. Compliance with GMP is mandatory to ensure product safety, efficacy, and quality, and to meet national and international regulatory requirements (such as WHO, US FDA, EU, ISO, and local authorities).
2. Objectives of the Training
The main objectives of GMP training are to:
· Build Awareness: Familiarize participants with GMP principles, regulations, and compliance requirements.
· Enhance Knowledge: Provide detailed understanding of manufacturing standards, documentation, and quality assurance.
· Ensure Compliance: Train staff to meet regulatory requirements and company SOPs.
· Promote Quality Culture: Develop good practices in hygiene, documentation, and production to ensure product integrity.
· Reduce Risks: Minimize contamination, errors, mix-ups, and recalls.
· Empower Employees: Define clear roles and responsibilities in achieving GMP standards.
3. Target Participants
GMP training is essential across different levels of an organization, especially in manufacturing-related industries. Target participants include:
· Production Staff (operators, supervisors, managers)
· Quality Control (QC) Personnel
· Quality Assurance (QA) Personnel
· Warehouse & Storekeepers (raw materials, finished goods)
· Engineering & Maintenance Team (equipment handling, calibration, maintenance)
· R&D and Technical Staff
· Regulatory Affairs Staff
· New Employees & Trainees (as part of induction/orientation)
· Middle & Senior Management (decision-makers responsible for compliance oversight)
4. Training Coverage (Key Topics)
· Introduction to GMP & regulations (WHO, FDA, EU, ISO, local authorities)
· GMP principles & quality culture
· Personnel responsibilities & hygiene practices
· Premises & equipment requirements
· Raw material handling & production controls
· Documentation & record-keeping (GDP, ALCOA+)
· Quality control & assurance systems
· Handling deviations, CAPA, change control
· Complaint handling & product recalls
· Warehousing & distribution requirements
· Case studies of GMP failures & lessons learned
Training Methods
· Classroom/Instructor-Led Training
· Interactive Workshops
o On-the-Job Training (OJT)
o E-Learning / Online Training
o Case Studies & Role Pla
· Quizzes & Assessments
· Group Discussions & Feedback Sessions
Registration Hotlines:
01739-138399
01312-138399
01824-576598
01772-825678
WhatsApp Number:
01739-138399
01312-138399
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Trainer:
Mohammad Abdur Rahman
Managing Director & Facilitator
Compliance Training (BD) Limited
Specialist Trainer & Consultant: Social & Technical Compliance
Writer: Compliance Series Books
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Registration Fee: BDT 3500/-
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Payment Modes:
Bkash A/C: 01739-138399 (Personal)
Nagad A/C: 01739-138399 (Personal)
DBBL Rocket A/C: 01739-1383997 (Personal)
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Card Number:0121 0845 8527
A/C Name: Mohammad Abdur Rahman
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A/C NAME: MOHAMMAD ABDUR RAHMAN
A/C NUMBER: 3001570018186
ROUTING NUMBER: 090262087
BRANCH: IBRAHIMPUR BANK: DUTCH-BANGLA BANK LTD.
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Email: compliancetrainingbd2019@gmail.com
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REGISTRATION HOTLINES
Mr. Mohammad Abdur Rahman is the country renowned Specialist Trainer of Social & Technical Compliance. He has long 16 years professional experience in HR, Admin & Compliance arena. He is the Freelance auditor, Team lead consultant also. He is the writer of compliance series books (9 Books) also. Good educational background & available practical professional job knowledge makes him an EXPERT in Compliance & HR arena. He is known as the compliance specialist in Bangladesh.
You are most welcome to communicate with us. We are always at your service.