As life sciences companies grow, the velocity needed to address organizational and regulatory demands often overwhelms internal capacity and resources.  

The need to leverage cross-disciplinary expertise becomes paramount to ensure that medical products and treatments fulfil utmost safety, quality and effectiveness while achieving agility and greater commercial success, now and in the future.    

At Qplus Consult, we bridge science, pharma-legislation, and business in helping our clients manage and minimize risks and position themselves to deliver real value and operational excellence. 

Since 2010, we thrive on building custom solutions for EU-based pharmaceutical and life science companies of all sizes, bringing together a tailored, multi-disciplinary team of professionals that fits the desired outcomes in the areas of: 

- Medical Affairs
- Pharmacovigilance
- Regulatory Affairs
- Quality Systems Management for PV, GMP, GDP or ISO 13485 and ISO 9001
- Quality Management and Auditing
- Learning Services via www.quastioncourses.com

Our success is gauged in terms of the results we drive for our clients, and we are bent on providing both quick and lasting wins. 

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Life Sciences

Qplus consult bv

Qplus consult bv's headquarters in Zaventem, Belgium

Kristina Bindus

This department focuses on assessing and managing the safety of pharmaceutical products throughout their lifecycle.

Qplus consult bv

Org chart

Teams

Drug Safety

Offices

Qplus consult bv

Org chart

Teams

Drug Safety

Offices

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