AqVida – Your Consultant for achieving GMP Compliance 

AqVida has been providing the know-how on achieving EU GMP compliance to its business partners and contract manufacturers. GMP compliance is a culture, and it requires many trials-and-errors to achieve. However, with proper guidance and consultation, the path to EU GMP compliance can be reached quickly and more efficiently.

There are many success stories for achieving EU GMP Compliance with the guidance from AqVida. Thanks to AqVida, manufacturing sites located in various continents - such as South Korea, India, Argentina, China, etc. - have successfully upgraded and passed EU GMP inspections and received GMP certificates.

 

Scope of consultation service includes

  • GMP consultation based on EU GMP, US cGMP, PIC/S, and WHO Guidelines

  • Evaluation of quality management system

  • Mock-inspection and Gap analysis (recommendation for correction and CAPA)

  • Supplier audit for GMP compliance as 3rd party auditor

  • Facility/Equipment design for oral solid dosage form and sterile injections

  • GMP Interpreter/Translator (English/German/Korean)

 

AqVida’s expertise in EU GMP compliance can help you upgrade your GMP system. Inquiry can be sent to the following e-mail address: dwight@aqvida.com. 

 

 

AqVida Production Site co-financed by EFRE

Headquarters:

AqVida GmbH

Kaiser-Wilhelm-Str. 89

20355 Hamburg

Germany

 

Manufacturing Site:

Werkstr. 21

23942 Dassow

Germany

Phone: +49 (0)40 38037190

Fax:     +49 (0)40 38037192

info@aqvida.com

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