ISO 22716

ISO 22716:2007 is an internationally recognized standard that provides comprehensive guidelines on Good Manufacturing Practices (GMP) specifically for the cosmetics industry. Developed by the International Organization for Standardization (ISO), this standard ensures the quality, safety, and traceability of cosmetic products throughout the entire production and distribution process.

Quality Asia Certification offers ISO 22716 certification services across India and beyond, helping cosmetic manufacturers, private labelers, and distributors align their operations with global GMP expectations. With the growing consumer awareness and regulatory requirements, obtaining ISO 22716 certification is now more than a compliance need—it's a business advantage.

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60% Sustainability

80%

Customer Attraction

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Increase Your Competitive Edge

What is ISO 22716?

ISO 22716:2007 is a GMP guideline tailored for cosmetic products, covering every aspect of manufacturing, packaging, testing, storage, and transportation. Unlike general quality standards, ISO 22716 focuses on practical, process-oriented guidance to ensure a controlled production environment that minimizes contamination, errors, and product defects.

This certification applies to organizations involved in:

  1. Manufacturing and packaging of cosmetic products
  2. Raw material sourcing and processing
  3. Quality control and testing laboratories
  4. Warehousing and distribution of cosmetics


Why is ISO 22716 important?

The cosmetic industry is highly regulated due to its direct impact on consumer health and safety. Regulatory bodies like the European Commission, FDA, and BIS (India) now expect cosmetic companies to demonstrate compliance with internationally accepted GMP guidelines. ISO 22716 certification satisfies this demand and enhances both market access and brand credibility.

Key reasons to opt for ISO 22716 certification:

  1. Mandatory in many global export markets including the EU
  2. Builds confidence among distributors, consumers, and regulatory authorities
  3. Supports product recalls, audits, and compliance reporting
  4. Reduces risk of contamination, quality complaints, and legal penalties
  5. Aligns with global supply chain expectations


What are the benefits of ISO 22716?

Implementing ISO 22716 standards equips your organization with well-defined processes, trained personnel, and systematic quality checks. Here are key internal benefits:

  1. Establishes clear standard operating procedures (SOPs)
  2. Promotes hygiene, cleanliness, and personnel discipline
  3. Controls raw material quality and traceability
  4. Minimizes human error with consistent documentation
  5. Enhances readiness for regulatory and third-party audits
  6. Boosts internal efficiency and reduces waste


What kind of businesses can benefit from ISO 22716?

Getting ISO 22716:2007 certification from Quality Asia Certification enables your cosmetic business to stay ahead in a competitive and regulated market. Here’s how your business benefits:

  1. Global Market Access: Certification enables smoother entry into international markets, particularly in the EU where GMP compliance is mandatory.
  2. Regulatory Confidence: Demonstrates compliance with international cosmetic regulations, reducing risk of product bans or penalties.
  3. Brand Trust & Credibility: Enhances consumer confidence in the safety and reliability of your products.
  4. Supply Chain Recognition: Builds trust with B2B partners like retailers, OEMs, and distributors who seek GMP-compliant suppliers.
  5. Reduced Operational Risks: Systematic controls reduce chances of contamination, product recalls, and customer complaints.
  6. Enhanced Reputation: A visible commitment to quality and safety enhances your brand image and consumer loyalty.
  7. Sustainability in Manufacturing: Promotes lean manufacturing practices, resource optimization, and environmental responsibility.


Top Tips on making ISO 9001 effective for you.

#1

Top management commitment while practicing and accomplishing the standard is the key to success.

#2

Keeping staff informed about the ongoing practices, a well-communicated plan would increase the motivation and zeal of working in them.

#3

Making sure that the various departments of the organization work as a team for the benefit of the organization and customers as well.

#4

Review systems, policies, processes, and procedures for a smooth working of QMS.

#5

Speaking to customers & suppliers while getting feedback & working on improvements.

#6

Training staff carrying out the internal audits with the opportunity for improvement.

#7

Celebrate your achievement and use the QualityAsia Assurance Mark on your literature, promotional material, and website.

#8

Ensure continuous improvement by regularly reviewing and updating your quality management practices.

#9

Promote a culture of quality by encouraging innovation, accountability, and employee involvement at every level of the organization.

Why QualityAsia?

QualityAsia always vanguard in the auditing and governing of internationally acclaimed standards practices. At QualityAsia, we focus on driving the success of our clients through creating excellence with our trained professional auditors. The content of our service provision, comply with international certification rules defined by the accreditation bodies without burning a hole in your pocket. We will take you through the journey of audits with our best kept audit practices, viz.:

Initial Certification – Stage 1 (Preparatory Phase)
  • Thorough documented information review.
  • Exchange of information with staff through online or onsite presence.
  • Identification of key performances, processes & objectives as per the standard requisites.
  • Analysis of facilities, infrastructure, systems and processes in regard with the requested certification scope with a resource allocation review.

Initial Certification – Stage 2 (On-site Audit)
  • Measurement, reporting & reviewing the performances against key performances objectives.
  • Reviewing the suitability of the system meeting the legal, regulatory & contractual requirements.
  • Operational control of processes, internal audits & management reviews while understanding the responsibilities for the policies.
  • Conclusion based on prescriptive requirements, policy, performance objectives, staff skill, operations, procedures, internal audits, etc.


    Surveillance & Certification Renewal

    Drawing out the scrutiny on various aspects of the previously done audits on effectiveness while reviewing the various processes and control of the operations in the QMS and finally going for the recertification.

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