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We are a network of experts in the EU GMP field, with the main goal is to help businesses in Southeast Asia’s pharmaceutical to meet the EU GMP standards.
The EU GMP Network (EGN) consists of leading experts in the field of GMP consulting for the pharmaceutical and medical device industries according to European standards (EMA).
We support our customers throughout the complete project lifecycle, starting from the point of project definition, continuing through implementation, qualification, validation, quality system maintenance and improvement.
EU GMP Network (EGN) not only has expertise in EU GMP but also has experience in consulting for many projects in Europe and Asia to achieve EU GMP certification. We also understand well about the market and the difficulties of Vietnamese pharmaceutical enterprises in the process of obtaining the EU GMP certificate. EGN is full of experience and knowledge of Asian culture, and has relationships with many pharmaceutical regulatory authorities in Europe, so we are ready to answer all your questions.
The question in the title “Are consultants a universal remedy?” is of course a bit provocative. Yet the sole involvement
The European Medicines Agency (EMA) has adopted the ICH guidance on the continuous manufacturing of drug substances and drug products
In Mid-November, the ICH Q13 Guideline on “Continuous Manufacturing of Drug Substances and Drug Products (Step 4)” was finally adopted
A pharmaceutical product must be of the best quality and must meet both good manufacturing and storage practices. Join us
Requirements on personnel training according to GMP EU regulations The manufacturer must have a training program for all employees involved
What is the cleanliness level of the cleanroom? Clean areas are controlled in terms of factors: the limit of particles
GMPnetwork.eu (ENG) is a network of EU GMP consultants with the main goal of helping Southeast Asian pharmaceutical businesses meet EU GMP standards.
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Ho Chi Minh, Vietnam
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