If your business manufactures food, pharmaceuticals, cosmetics, supplements, chemicals, or medical products, your customers expect consistent quality and product safety. Without a GMP (Good Manufacturing Practices) system, your business risks:
With GMP Certification, your business becomes audit-ready, quality-driven, and globally trusted.
ISO 13485 is the international Quality Management System standard for medical devices. It ensures product safety, risk control, process consistency, and regulatory compliance—which is mandatory to meet CE Marking (Europe), FDA 21 CFR 820 (USA), Health Canada, and other medical regulations.
Our ISO 13485 Consulting Approach – Practical, Regulatory-Compliant & Audit Ready
At Greendot Consulting, we believe certification should add value, not paperwork. We build systems that work on the shop floor, not just the audit table.
GMP (Good Manufacturing Practices) is a globally recognized quality system that ensures products are consistently produced and controlled according to defined standards of safety, hygiene, and regulatory compliance.
GMP covers:
GMP is essential for industries where product safety and hygiene are critical:
Industry | Application |
Pharmaceuticals | Tablets, syrups, capsules, injectables |
Nutraceuticals & Supplements | Protein powder, herbal products |
Cosmetics & Personal Care | Shampoo, cream, lotions |
Food & Beverages | Dairy, snacks, bakery, beverages |
Chemical Manufacturing | Specialty and industrial chemicals |
Medical Devices | Components & finished products |
Veterinary Products | Animal health products |
If you sell to export markets or premium buyers, GMP Certification is a must.
Why GMP Matters
Without GMP | With GMP Certification |
Frequent customer complaints | Higher product consistency |
Risk of contamination | Hygienic & controlled production |
Regulatory warnings | Compliance confidence |
Low buyer trust | Increased customer credibility |
No system for recalls | Strong traceability & risk control |
Limited growth | Entry into export & new markets |
Practical. Systematic. Result Oriented.
We don’t believe in heavy paperwork or complicated templates. We build simple, scalable, and compliance-ready systems.
Our 6-Step GMP Certification Process
Audit of current production, hygiene & quality practices
Customized plan based on your factory setup
SOPs, quality manuals, checklists, logs, forms
Material flow, cross-contamination control, 5S hygiene
Workforce training for GMP best practices
Pre-audit review + support with certification body selection
We support compliance with:
Whether you are upgrading your quality system or preparing for global buyers—we are your partner in compliance and operational excellence.
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