What Is WHO-GMP Certification and Why Every Manufacturer Needs It

In today’s worldwide pharmaceutical and healthcare manufacturing industry, the product quality, safety, and testing are non-negotiable. Every pharma manufacturer goes with medicine, nutrients, cosmetics range, and various healthcare products under the WHO-GMP certifications. Most countries only accept WHO-GMP-verified healthcare and pharmaceutical products. WHO-GMP is considered the verified certification for building brand goodwill. In this article, we will explore What Is WHO-GMP Certification and Why Every Manufacturer Needs It.

Key stats of WHO-GMP certified manufacturers in India

As per the study of central drugs standard control organisation, the total WHO-GMP certified manufacturing units of pharmaceutical products are 1329.

What is WHO-GMP Certification?

WHO-GMO certifications stand for the World Health Organisation and Good Manufacturing Practices for ensuring product manufacturing quality standards. These certifications ensure the pharmaceutical products are manufactured to strict quality standards and testing as per the regulations of international quality benchmarks.

WHO-GMP covers critical areas like:

• Raw material sourcing
• Storage & distribution
• Production processes
• Packaging & labelling
• Quality control testing
• Facility cleanliness & maintenance
• Equipment validation
• Documentation & batch records
• Staff hygiene & training

Why Are WHO-GMP Certifications Important For Every Manufacturer?

These global certifications are essential for every manufacturer because every pharmaceutical product meets global safety regulations and ingredient purity standards. These certifications easily build trust among every international buyer to enhance market access and increase market goodwill of pharma products or manufacturers.

Certified manufactured products are easy to import and export to other countries without any regulatory expectations.

• Global market access: Most countries require WHO-GMP certifications to import and export medical or healthcare products. Avoiding these certificates, most companies lose out on supplying the global procurement and international market.
• Boosts product quality: these global certificates ensure the quality of the manufacturing unit at every step by reducing manufacturing errors, contamination risks, or batch failures.
• Build customer trust: these certifications enhance customer trust and market goodwill because WHO-GMP is known for quality assurance, and every brand follows WHO health guidelines.
• Boosts Brand Reputation: WHO-GMP certifications easily build customer trust because they are known for the best quality checks and assurance.
• Reduces Costs & Waste: Most of the manufacturers take these certificates and experience fewer recalls, deviations, and standard breakdowns.
• Beneficial for international tenders: Most of the government healthcare programs, NGOs, or countries only support WHO-GMP-approved manufacturers.
• Regulatory compliance: the best certification structure works with regulatory standards and the World Health Organization’s schemes.

What Are The Key Requirements Of WHO-GMP Certifications?

Every pharmaceutical manufacturer needs several guidelines, including:

• Most of the industries need to maintain layout and gyne standards.
• Manufacturers need to ensure the machines work more accurately.
• Follow the SOPs procedure and detailed documentation for every process.
• Ensure the QC and QA processes run smoothly in your facility, like raw material and finished goods.
• Proper records of every batch with reports, testing, and material quantity usage
• Workers’ training to maintain hygiene and safety protocols.
• Validation or qualification for reducing product recall & complaint handling system.

Which industrial manufacturers need WHO-GMP certifications?

WHO-GMP certifications are not only for quality testing and product safety, but they’re also all about customer, patient trust and following safety regulatory standards.

• Pharmaceuticals
• Manufacturing industry
• Cosmetics
• Medical devices
• Disposable health products
• Drugs and the active pharmaceutical industry.
• Disinfectants and sanitization industries

What Are The key Benifits of Owning WHO-GMP Certifications?

Benefits	Explanation
Increase Global Credibility	Every customer trusts WHO-GMP-certified brands for ensuring safety standards.
Boosts Global International Business Expansion	Important for exporting and importing medicine for global markets.
Increase Operational Efficiency	It standardizes all the procedures by reducing errors, downtime, and wastage.
Ensure Product Efficiency	It ensures every batch maintains the safety, purity, and work performance level.
Enhance Customer Satisfaction	Easily builds customer trust and a healthy relationship with manufacturers with products.
Reduce Risks	Cross-mixing, equipment issues, and reducing safety risks

Why Choose Lifevision Healthcare for WHO-GMP-verified medical Or Healthcare Products?

When it talks about the pharmaceutical industry, LifeVision Healthcare stands out as the most trusted or reputable medical or healthcare products supplier. Choosing LifeVision Healthcare means partnering with reliable, quality-driven driven and internationally recognized pharma manufacturers.

People Also Ask About What the WHO-GMP Certification is and why Every Manufacturer Needs it.

Q.1 Does WHO-GMP certification have expiry dates?

A: The WHO-GMP certificates have expiry dates or need renewal as per the missing authority. These WHO-GMP certificates are valid for 3 to years.

Q.2 How much does it cost to own these certificates for the pharma manufacturing industry?

A: The cost starts from getting ranges between 1.5 lacks to 10 lacks. Depend on the industry size or audit requirements.

Q.3 How long does it take for approval of these certifications?

A: Manufacturing of WHO-GMP certificates usually takes 2 to 6 months, but it depends on your applications and audit results.

Q.4 How does this certificate help to improve product quality or safety?

A: It enhances product quality, safety, hygiene, documentation, and testing of the manufacturing process.