Regulatory Affairs & Drug Development from the selection of a promising drug to regulatory submission of all generated data. Several, quite diverse disciplines are involved and external integrated approach being an extension of your objectives would bring added value for submission or due diligence.


By teaming up with LRSS, YOU as the client may expect:

• focus on and first priority to your specific needs

• input based on extensive experience in Regulatory Affairs & Drug Development, obtained in

several therapeutic areas and for several Regulatory pathway

• quality documents at a competitive price within pre-agreed timelines