{"id":30,"date":"2019-10-30T08:05:16","date_gmt":"2019-10-30T08:05:16","guid":{"rendered":"https:\/\/demo.casethemes.net\/consultio-corporate3\/?page_id=30"},"modified":"2025-11-16T23:22:26","modified_gmt":"2025-11-16T20:22:26","slug":"faq","status":"publish","type":"page","link":"https:\/\/qualityacademia.com\/en\/faq\/","title":{"rendered":"FAQ"},"content":{"rendered":"\t\t
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\r\n \r\n \r\n You can learn more from our asked questions\r\n \r\n <\/span>\r\n <\/h3>\r\n <\/div>\r\n<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t <\/div>\n <\/div>\n
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From our Frequently Asked Questions (FAQ) section, you can gain more information about our services, products, or processes, quickly resolve any questions you may have, and better understand how our processes work.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t <\/div>\n <\/div>\n <\/div>\n <\/section>\n

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\r\n \r\n What is GDP consultancy and why is it important? <\/i>\r\n <\/a>\r\n <\/div>\r\n

GDP consultancy provides expert guidance to ensure that pharmaceuticals and medical devices are distributed safely, efficiently, and in compliance with regulations. This is critical for maintaining product integrity and patient safety.<\/p><\/div>\r\n <\/div>\r\n

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\r\n \r\n How long does the consultancy take? <\/i>\r\n <\/a>\r\n <\/div>\r\n

Duration depends on company size and current compliance level; typically, an intensive program of 4\u201312 weeks is implemented.<\/p><\/div>\r\n <\/div>\r\n

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\r\n \r\n Why is GMP consultancy necessary? <\/i>\r\n <\/a>\r\n <\/div>\r\n

GMP consultancy ensures that manufacturing processes comply with legal and international standards, guaranteeing quality and patient safety.<\/p><\/div>\r\n <\/div>\r\n

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\r\n \r\n Why are validation services conducted? <\/i>\r\n <\/a>\r\n <\/div>\r\n

To ensure product quality, meet regulatory requirements, and minimize operational risks.<\/p><\/div>\r\n <\/div>\r\n <\/div>\r\n \t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t <\/div>\n <\/div>\n

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\r\n \r\n What is end-to-end validation? <\/i>\r\n <\/a>\r\n <\/div>\r\n

It is a comprehensive validation process covering operations, equipment, cleaning, computerized systems, and analytical methods.<\/p><\/div>\r\n <\/div>\r\n

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\r\n \r\n Which industries require GMP compliance? <\/i>\r\n <\/a>\r\n <\/div>\r\n

It applies to all companies operating in pharmaceuticals, biotechnology, medical devices, and healthcare manufacturing.<\/p><\/div>\r\n <\/div>\r\n

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\r\n \r\n What benefits can I get from GMP consultancy? <\/i>\r\n <\/a>\r\n <\/div>\r\n

Regulatory compliance, production efficiency, risk reduction, and sustainable business success are the main benefits.<\/p><\/div>\r\n <\/div>\r\n

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\r\n \r\n How is a science-based and risk-driven approach applied? <\/i>\r\n <\/a>\r\n <\/div>\r\n

Each process is analyzed through risk assessment and scientific evaluation, turning validation from a regulatory requirement into a strategic tool for quality and compliance.<\/p><\/div>\r\n <\/div>\r\n <\/div>\r\n \t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t <\/div>\n <\/div>\n <\/div>\n <\/section>\n

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\r\n \r\n \r\n Do you still have any problems with the solutions?\r\n \r\n <\/span>\r\n <\/h3>\r\n <\/div>\r\n<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t <\/div>\n <\/div>\n
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Do you still have any issues with the solutions we provided, or need further support or clarification? We want to ensure everything is working perfectly for you.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t <\/div>\n <\/div>\n <\/div>\n <\/section>\n

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\r\n Head office address: <\/h3>\r\n
Maslak Mah. Maslak Meydan Sk. Beybi Giz Plaza A Blok No.: 1 \u0130\u00e7 Kap\u0131 No.: 99 Kat: 26-27 Sar\u0131yer-\u0130stanbul\n<\/div>\r\n <\/div>\r\n<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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(+90) 212 335 64 05
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\r\n Mail for information: <\/h3>\r\n
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