Pharmaceutical Manufacturing: Best Practices and Compliance

Course Overview

  • Understand the principles and processes involved in pharmaceutical manufacturing.
  • Learn best practices for ensuring product quality, safety, and regulatory compliance.
  • Explore Good Manufacturing Practices (GMP) and quality assurance systems.
  • Gain practical knowledge to improve operational efficiency, compliance, and risk management in pharmaceutical production.

Training Format:In-class, Virtual, In-house

Location:Lagos, Accra, Nairobi, Kigali

Language:English, French

Nigeria Price:
₦350000

Int'l., (Nigeria) Price:
$1000

Ghana Price:
$4000

Kenya Price:
$5500

Rwanda Price:
$6000

Nigeria Price:₦350000

Int'l., (Nigeria) Price:
$1000

Ghana Price:
$4000

Kenya Price:
$4000

Rwanda Price:
$4000

Nigeria Price: ₦350000

Int'l., (Nigeria) Price:
$1000

Ghana Price: $4000

Kenya Price: $4000

Rwanda Price: $4000

Introduction to Pharmaceutical Manufacturing

  • Overview of Pharmaceutical Production: Types of products (tablets, capsules, injectables, biologics).
  • Manufacturing Processes: Formulation, processing, packaging, and distribution.
  • Industry Challenges: Quality control, regulatory requirements, and safety concerns.

Good Manufacturing Practices (GMP)

  • Principles of GMP: Ensuring product quality, safety, and consistency.
  • Regulatory Standards: WHO, FDA, and local regulatory requirements.
  • Documentation and Record Keeping: Batch records, SOPs, and traceability.

Quality Assurance and Quality Control

  • Quality Assurance Systems: Policies, procedures, and compliance frameworks.
  • Quality Control Testing: Raw materials, in-process checks, and finished products.
  • Validation and Qualification: Equipment, processes, and cleaning validation.

Production and Process Optimization

  • Manufacturing Operations: Process flow, equipment usage, and standardization.
  • Process Optimization: Improving efficiency and reducing waste.
  • Automation and Technology: Digital systems and smart manufacturing solutions.

Risk Management and Compliance

  • Risk Identification: Contamination, deviations, and product recalls.
  • Compliance Audits: Internal and external inspections.
  • Corrective and Preventive Actions (CAPA): Managing deviations and improvements.

Health, Safety, and Environmental Management

  • Workplace Safety: Handling chemicals and hazardous materials.
  • Environmental Controls: Waste management and pollution control.
  • Occupational Health: Protecting workers and ensuring safe operations.

1ST BATCH: Tuesday, March 24, 2026 — Friday, March 27, 2026.

2ND BATCH: Tuesday, July 21, 2026 — Friday, July 24, 2026.

3RD BATCH: Tuesday, December 8, 2026 — Friday, December 11, 2026.

The training methodology integrates lectures, interactive discussions, collaborative group exercises, and
illustrative examples. Participants will acquire a blend of theoretical insights and hands-on practical
experience, emphasizing the application of learned techniques. This approach ensures that attendees return
to their professional environments equipped with both the competence and self-assurance to effectively
implement the acquired skills in their responsibilities.

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