AqVida - your competent advisor for all aspects of GMP standards

GMP stands for Good Manufacturing Practice. It incorporates rules and guidelines to control and guarantee quality in pharmaceutical, cosmetics or food production. Especially when producing pharmaceutical products, GMP including quality assurance plays a central role—ultimately in protecting patient health and safety. Major GMP Guidelines are provided by such national authorities as European Commission and US FDA and by international committees such as ICH and PIC/S.


AqVida has been providing the know-how on achieving GMP compliance to its business partners and contract manufacturers since 2011. Our mutual aim is to align your GMP system with EU GMP.

AqVida – your consultant for achieving GMP compliance

GMP stands for Good Manufacturing Practice. It incorporates rules and guidelines to control and guarantee quality in pharmaceutical, cosmetics or food production. Especially when producing pharmaceutical products, GMP including quality assurance plays a central role - ultimately in protecting patient health and safety. Major GMP Guidelines are provided by such national authorities as European Commission and US FDA and by international committees such as ICH and PIC/S.

 

AqVida has been providing the know-how on achieving GMP compliance to its business partners and contract manufacturers since 2011. Our mutual aim is to align your GMP system with EU GMP.

Dwight You

 GMP compliance is a culture. 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. AqVida’s expertise in EU GMP compliance can help you upgrade your GMP system. Please send your inquiry:
Write to me!

Dwight You

GMP compliance is a culture. 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. AqVida’s expertise in EU GMP compliance can help you upgrade your GMP system. Please send your inquiry:
Write to me!

AqVida supports you to enhance your GMP system.

Our scope of consultation services 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 supports you to enhance your GMP system.

Our scope of consultation services 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)

References

There are many success stories of achieving EU GMP compliance with the help of AqVida advice. Thanks to AqVida, production facilities on various continents and in countries such as South Korea, India, Argentina, China and Ukraine have successfully passed the EU's GMP inspections and received GMP certificates. Some of these companies also became our manufacturers and suppliers, whom we regularly inspect with the German authorities.

References

There are many success stories for achieving EU GMP Compliance with the guidance from AqVida. Thanks to AqVida, manufacturing sites located in various continents and countries such as South Korea, India, Argentina, China, etc. have successfully upgraded and passed EU GMP inspections and received GMP certificates. Some became our manufacturers and suppliers, to which we travel with our German authority to inspect regularly.

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