GMP (Good Manufacturing Practices) is an internationally recognized system that ensures products are consistently produced and controlled according to strict quality standards. It focuses on eliminating risks in production, such as contamination, errors, and deviations.
GMP guidelines cover everything from facility hygiene and equipment maintenance to staff training and documentation practices.
We review your current processes against ISO 9001 requirements to identify gaps and improvement areas.
A preliminary evaluation is conducted to ensure your system is aligned with ISO standards before the formal audit.
Internal audits are performed and staff are trained to ensure readiness for certification.
An accredited auditor performs the official assessment to verify full compliance with ISO requirements.
Upon successful audit completion, your organization receives an internationally recognized ISO certificate.
Surveillance audits ensure ongoing compliance and continuous improvement.
Improve product quality, ensure safety, and reduce waste through controlled production processes.
Strengthen quality assurance practices and increase credibility when bidding for large-scale projects.
Improve patient safety, strengthen hygiene standards, and ensure safe handling of critical medical products.
Enhance process consistency, data integrity, and reliability — crucial for companies developing regulated software or medical/industrial applications.
Improve supply chain controls, ensure product authenticity, and boost customer satisfaction.
Ensure safety, reduce operational risks, and maintain high-quality standards in chemical handling and production processes.
A quality assurance system ensuring products are consistently produced according to safety and quality standards. GMP is widely required by MOH (UAE), and other GCC regulatory bodies.
Food, cosmetics, pharmaceuticals, and supplement manufacturers.
In many sectors, yes — especially pharmaceuticals.
Cleanliness, documentation, hygiene, equipment control, and personnel training.
Usually 4–10 weeks.
Contact Callids Global today for a free consultation & quote.
Callids Global is an accredited certification body that issues internationally recognized accredited certificates to companies in a wide range of manufacturing and service industries attesting to compliance with various national and international regulatory standards.
Check the authenticity of any ISO certificate in just one click.
UAE
M Floor, Remah Towers, Al Khalidiyah,
Abu Dhabi, United Arab Emirates
INDIA
Senate Space, UR Nagar Extension, Anna Nagar West Extn, Chennai, Tamil Nadu, India - 600050
UNITED STATES
Registered Accreditation Office 8 The Green, Dover, DE, 19901, United States
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