GMP for Cosmetic Products - Comply with ISO 22716


Instructor: Mohammad Elnadi
Product ID: 705788

  • Duration: 90 Min
This webinar will discuss the requirements, clauses and steps to comply with ISO 22716. It will help you understand how to maintain the quality of your products.
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Why Should You Attend:

Since the release of the international standard ISO 22716, several regulatory bodies are committed to adopt the ISO 22716 to introduce it to their regions of authority. Not only manufacturers of cosmetics that need to be aware of this requirements but extends also to distributors and importers of these products and they are required to comply with this international standard. ISO 22716 for cosmetics industry assures quality of your products in terms of production, control, storage and shipment of cosmetic products.

Attend this webinar to :

  • Understand the importance of complying with the international standard for your business
    • Business requirement
    • Regulatory requirement
    • Quality requirement
  • Understand the clauses of ISO 22716
  • Understand the steps to comply with ISO 22716

Areas Covered in the Webinar:

  • Why I need to comply with the international standards
    • Business requirement
    • Regulatory requirement
    • Quality requirement
  • Scope of ISO 22716 including
    • Personnel
    • Premises & equipments
    • Production
    • Quality control
    • Quality systems
  • How to comply with ISO 22716

Who Will Benefit:

  • Personnel involved in the cosmetics manufacturing operations including:
    • General management
    • Quality Assurance personnel
    • Quality Control personnel
    • Regulatory personnel
    • Production Personnel
  • Importers and distributors of cosmetics
Instructor Profile:
Mohammad Elnadi

Mohammad Elnadi
Co Founder and Managing Director, REYADA PRO Consulting Co.

Mohammad has a unique blend of both technical and business experience and qualifications. After graduating in pharmaceutical science, he has held posts in the fields of R&D and production of pharmaceutical dosage forms and as a toll manufacturing coordinator then, after completing postgraduate certificate in management from AUC, he has senior management roles in business development in pharmaceutical industry mainly in the area of planning, supply chain, process management & improvement and business excellence models and he leads teams for different QMS inspections as GMP & ISO 9001 inspections.

During his career in supply chain, he took the responsibility of establishing & structuring the supply chain department within the company to cover production planning, inventory control, distribution inside & outside Egypt for pharmaceutical companies.

During his career life, he conducted a lot of training sessions as internal training instructor for his team & as QMS consultant & instructor in REYADA PRO Consulting Co.

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