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İstanbul, Turkey

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Hakkında

2007 yılından bu yana, Quality Academia, ilaç, biyoteknoloji, tıbbi cihaz ve sağlık sektörlerindeki ulusal ve uluslararası kuruluşlara üst düzey mühendislik, denetim ve danışmanlık hizmetleri sunmaktadır. Avrupa, Orta Doğu ve Afrika’da faaliyet gösteren yüksek nitelikli mühendis, mimar, süpervizör ve danışman ekibimizle, Anahtar Teslim Tesis Projeleri ve GMP–GDP Uygunluk & Denetim Hizmetleri alanlarında uzman çözümler sağlamaktayız.

Quality Academia

2007

With a selection of our thought
leadership white papers by some
of the world’s leading

With a selection of our thought
leadership white papers by some
of the world’s leading

With a selection of our thought
leadership white papers by some
of the world’s leading

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See how we work with touch of experience

Why choose us

You have many reasons to choose but why Quality Academia

Because Quality Academia combines an expert multidisciplinary team, global experience, proven reliability, and strong regulatory compliance to provide high-quality, results-oriented solutions in every project we undertake.

Globally Recognized Certification Programs

Earn internationally valid Exemplar Global–approved certificates and become a certified GMP Lead Auditor recognized worldwide.

Full Compliance with Global Regulations

Our training and consultancy services are fully aligned with FDA, EMA, PIC/S, WHO, ICH, and EU GMP Annex 1guidelines — ensuring your operations meet the latest regulatory expectations.

Turnkey Facility Setup & Qualification

From concept to qualification, we deliver complete facility solutions including design, equipment selection, installation, DQ–IQ–OQ–PQ qualification, and full validation documentation.

Validation & Quality System Consultancy

We provide expert support for process, cleaning, method, software, and transport validations, as well as GMP, GDP, and Data Integrity system implementation and gap closure.

Industry-Leading Experts

Our trainers and consultants bring 20+ years of real-world experience in auditing, quality assurance, validation, and regulatory compliance within the pharmaceutical and biotechnology sectors.

Practical, Case-Based Learning

Each program includes audit simulations, case studies, and real GMP scenarios, bridging the gap between theory and real-life application.

Flexible & Comprehensive Service Models

We offer online, hybrid, and on-site solutions — covering training, auditing, consultancy, and project management under one roof.

Trusted by Global and Local Partners

Leading pharmaceutical, biotechnology, and medical device companies across Turkey and Europe trust us with their compliance and training projects.

Continuous Growth & Post-Project Support

Our partnership doesn’t end with delivery. We ensure sustainable success through graduate portals, refresher modules, re-certification programs, and ongoing consultancy support.

We have over 18 years experience

Since its establishment in 2007, our company has been delivering professional solutions to numerous national and international clients across various industries, including pharmaceuticals, biotechnology, medical devices, and healthcare services.

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Successfull Project

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Happy Clients

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Happy Customers

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Quality Staff

Customer experiences that inspire trust and drive growth.

Trusted by clients since 2007, Quality Academia has been a reliable partner for national and international organizations across the pharmaceuticals, biotechnology, medical devices, and healthcare industries. 

Schedule a meeting!

We’d love to hear from you and discuss how our expert team can help achieve your goals. Get in touch today!

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    Frequently Asked Questions

    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.

    Duration depends on company size and current compliance level; typically, an intensive program of 4–12 weeks is implemented.

    GMP consultancy ensures that manufacturing processes comply with legal and international standards, guaranteeing quality and patient safety.

    It is a comprehensive validation process covering operations, equipment, cleaning, computerized systems, and analytical methods.

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