ABOUT AQVIDA
AqVida is focussing on the development of innovative products, particularly high barrier to entry generics and biosimilars. Expert scientist compile dossiers in CTD format and DMFs for regulated and less regulated markets, and our experienced multinational regulatory affairs team provides high competence. They also do have direct contacts to regulatory authorities and a strong track record of completed registration procedures. AqVida‘s further business development activities include the search and selection of potential partners for:

• Sourcing of API with corresponding documentation
• Product licensing and supply
• Distribution of AqVida products in selected territories

AqVida applies a quality management system that is adhering to German legal requirements for the pharmaceutical industry (i.e. AMG and AMWHV). We have a strict quality system in place, assuring that all suppliers are compliant with EU-GMP regulations and our office in China is regularly carrying out audits and inspections for ongoing supplier qualification.

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