DRA Consulting Oy | Pakkalankuja 7 | FI-01510 Vantaa | +358 9 825 64 200 | info@dra.fi | www.dra.fi

It’s not magic, it’s expertise

Pharmaceutical and Chemical Services

Contact us:

Eija Hartikainen

Tel. +358 9 825 64 242

eija.hartikainen@dra.fi

Our service package includes

A smoother marketing authorisation process and more rapid market access are based on adequate

and clearly written, but not too extensive or detailed documentation. Unnecessary details increase the

number of future variation applications. Our specialists are at hand to help you avoid this.

DRA Consulting’s team specializes in writing pharmaceutical-chemical documentation and offers

expertise based on years of experience of the evaluation of applications both at Fimea (Finnish Medicines

Agency) and EDQM. We are uniquely placed to assess your marketing authorisations, variations or CEP

applications from the authorities’ viewpoint.

When you want to ensure that your application documentation is up to the right standard or if you need

additional capacity or expertise for writing your documentation, contact us. We are happy to help you!