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them are the European Good Manufacturing Practice (GMP) and ISO 9001: 2015. Our medical devices also meet the highest standards of the European Union and have acquired the CE marking. Vision Striving to become a global leader in the pharmaceutical industry, we aim for excellence in quality, integration of innovative technologies and we
Basic Clean Room Requirements | Designs for GMP Clean Rooms
In a pharmaceutical sense, clean rooms are those rooms that meet the code of GMP requirements as defined in the sterile code of GMP, i.e. Annex 1 of both the EU and PIC/S Guides to GMP and other standards and guidance as required by local health authorities.
Good Manufacturing Practice (GMP) Audits - Globi-Reg
This guideline describes the following points; Overview; Eligibility for Registration; Route of evaluation; The Registration process; Administrative information
NSF International | The Public Health and Safety Organization
NSF International protects and improves global human health. Manufacturers, regulators and consumers look to us to facilitate the development of public health standards and provide certifications that help protect food, water, consumer products and the environment.
Employee Archive - Quality Solutions NowQuality Solutions Now
Consultant. (610) 462-4090. email@example.com. Professional with pre-clinical/concept through product launch experience in quality systems, quality management, quality assurance and engineering, contract manufacturing, and operations. Over 39 years working with drug, medical device, combination, and consumer products manufacturers.