Regions  

About Us

XPforte is a professional R&D and Regulatory solutions provider. We develop and design solutions around the needs of the ever expanding global drug discovery and development clients to the global standards with a dedicated team of experts.

Our Ethos & Values

Our aim is to offer companies of all sizes a tailored, quality, adaptable and compliant solutions to their R&D and Regulatory needs that are timely and cost-efffective.

We are driven by AMBITION

A- Adaptability to the client needs

M- Management of the project by an expert

B- We intend to provide you with the Best support

I- Integrity of our appraisals to ensure they are honest ,
cost-conscious and have realistic deadlines

T- Timelines are met

I- Individual approach compared to other regulatory service providers

O- Openness with client to ensure that there is transparency on all aspects of the project.

N- Nurturing long-term relationships

N- Nurturing long-term relationships

We are driven by Ambition

  • A – Adaptability to the client needs
  • M – Management of the project by an expert
  • B – We intend to provide you with the Best support
  • I – Integrity of our appraisals to ensure they are honest cost-conscious and have realistic deadlines
  • T – Timelines are met
  • I – Individual approach compared to other regulatory service providers
  • O – Openness with client to ensure that there is transparency on all aspects of the project.
  • N – Nurturing long-term relationships

Our Team

We have started as a group of professionals with several decades of professional consulting experience.

XPForte has a team of experts ready to provide support and advice for any questions or special requests you may have, so feel to give us a call if you are in need.

Joseph Irwin
Director

Joseph has 30 years of industry R&D experience developing drugs. He has extensive experience in global drug development, regulatory strategy and commercialisation of various products for early stage to bluechip biotech and pharma companies.

Adnan Ahmed
Director

Adnan has 20 years of regulatory & commercial experience successfully contributing to the global regulatory affairs and commercialisation of various products.

Fouzia Naveed
Director

Fouzia has 18 years of experience in R&D regulatory affairs across multiple therapeutic areas. She has broad experience in regulatory strategy, clinical trials and operations.